Intersex medical interventions

From Wikipedia, the free encyclopedia
  (Redirected from Intersex surgery)
Jump to: navigation, search

Intersex medical interventions are surgical, hormonal and other medical interventions performed to modify atypical or ambiguous genitalia and other sex characteristics, primarily for the purposes of making a person's appearance more normal and to reduce the likelihood of future problems. The history of intersex surgery has been characterized by controversy due to reports that surgery can compromise sexual function and sensation, and create lifelong health issues.[1][2] Timing, evidence, necessity and indications for surgeries in infancy, adolescence or adult age have been controversial, associated with issues of consent.

Interventions on intersex infants and children are increasingly recognized as human rights issues. Intersex organizations, and human rights institutions increasingly question the basis and necessity of such interventions.[3][4] In 2011, Christiane Völling won the first successful case brought against a surgeon for non-consensual surgical intervention.[5] In 2015, the Council of Europe recognized, for the first time, a right for intersex persons to not undergo sex assignment treatment[6] and Malta became the first country to prohibit involuntary or coerced modifications to sex characteristics.[7][8][9]

Purposes of genital reconstructive surgery[edit]

The goals of surgery vary with the type of intersex condition but usually include one or more of the following:

Physical health rationales:

Psychosocial rationales:

  • to alleviate parental distress over the atypical genital appearance.
  • to make the appearance more normal for the person's sex of rearing
  • to reduce effects of atypical genitalia on psychosexual development and gender identity
  • to improve the potential for adult sexual relationships

Both sets of rationales may be the subject of debate, particularly as the consequences of surgical interventions are lifelong and irreversible. Questions regarding physical health include accurately assessing risk levels, necessity and timing. Psychosocial rationales are particularly susceptible to questions of necessity as they reflect social and cultural concerns. There remains no clinical consensus about an evidence base, surgical timing, necessity, type of surgical intervention, and degree of difference warranting intervention.[10][11][12] Such surgeries are the subject of significant contention, including community activism,[13] and multiple reports by international human rights[6][14][15][16] and health[1] institutions and national ethics bodies.[3][17]

Types of intervention[edit]

Interventions include:

  • surgical treatment
  • hormone treatment
  • genetic selection and terminations
  • treatment for gender dysphoria
  • psychosocial support

Surgical interventions can broadly be divided into masculinizing surgical procedures intended to make genitalia more like those of typical XY-males, and feminizing surgical procedures intended to make genitalia more like those of typical XX-females. There are multiple techniques or approaches for each procedure. Some of these are needed for variations in degrees of physical difference. Techniques and procedure have evolved over the last 60 years. Some of the different techniques have been devised to reduce complications associated with earlier techniques. There remains a lack of consensus on surgeries, and some clinicians still regard them as experimental.[18]

Some children receive a combination of procedures. For example, a child regarded as a severely undervirilized boy with a pseudovaginal perineoscrotal hypospadias may have midline urogenital closure, third degree hypospadias repair, chordee release and phalloplasty, and orchiopexy performed. A child regarded as a severely virilized girl with congenital adrenal hyperplasia (CAH) may undergo both a partial clitoral recession and a vaginoplasty.

Masculinizing surgical procedures[edit]

Orchiopexy and hypospadias repair are the most common types of genital corrective surgery performed in infant boys. In a few parts of the world 5-alpha-reductase deficiency or defects of testosterone synthesis, or even rarer forms of intersex account for a significant portion of cases but these are rare in North America and Europe. Masculinizing surgery for completely virilized individuals with XX sex chromosomes and CAH is even rarer.

Orchiopexy for repair of undescended testes (cryptorchidism) is the second most common surgery performed on infant male genitalia (after circumcision). The surgeon moves one or both testes, with blood vessels, from an abdominal or inguinal position to the scrotum. If the inguinal canal is open it must be closed to prevent hernia. Potential surgical problems include maintaining the blood supply. If vessels cannot be stretched into the scrotum, or are separated and cannot be reconnected, a testis will die and atrophy.

Hypospadias repair may be a single-stage procedure if the hypospadias is first or second degree (urethral opening on glans or shaft respectively) and the penis is otherwise normal. Surgery for third degree hypospadias (urethral opening on perineum or in urogenital opening) is more challenging, may be done in stages, and has a significant rate of complications and unsatisfactory outcomes.[19] Potential surgical problems: For severe hypospadias (3rd degree, on perineum) constructing a urethral tube the length of the phallus is not always successful, leaving an opening (a "fistula") proximal to the intended urethral opening. Sometimes a second operation is successful, but some boys and men have been left with chronic problems with fistulas, scarring and contractures that make urination or erections uncomfortable, and loss of sensation. It is increasingly recognized that long-term outcomes are poor.[20][21]

Epispadias repair may involve comprehensive surgical repair of the genito-urinary area, usually during the first 7 years of life, including reconstruction of the urethra, closure of the penile shaft and mobilisation of the corpora.

Urogenital closure closure of any midline opening at the base of the penis. In severe undervirilization a boy may have a "pseudovaginal pouch" or a single urogenital opening in the midline of the perineum. Potential surgical problems: The most complicated aspect of closure involves moving the urethra to the phallus if it is not already there (i.e., repairing a perineal hypospadias). Fistulas and scarring are the main risks. Loss of sensation.

Gonadectomy (also referred to as "orchiectomy") removal of the gonads. This is done in three circumstances. (1) If the gonads are dysgenetic testes or streak gonads and at least some of the boy's cells have a Y chromosome, the gonads or streaks must be removed because they are nonfunctional but have a relatively high risk of developing gonadoblastoma. (2) In rare instances when an XX child has completely virilizing congenital adrenal hyperplasia (Prader stage 5), the ovaries can be removed before puberty to stop breast development and/or menstruation. (3) Gonadectomy can be performed in the equally rare instance of a child with true hermaphrodite virilized enough to raise as male, in which ovaries or ovotestes can be removed. Potential surgical problems: A lifetime of hormone replacement will be required, to avoid osteoporosis and enable sexual functioning.

Chordee release is the cutting of ventral penile skin and connective tissue to free and straighten the penis. A mild chordee, manifest as a well-formed penis "bent" downward by subcutaneous connective tissue, may be an isolated birth defect easily repaired by releasing some of the inelastic connective tissue on the ventral side of the shaft. In a complete chordee the phallus is "tethered" downward to the perineum by skin. A more severe chordee is often accompanied by a hypospadias and sometimes by severe undervirilization: a perineal "pseudovaginal pouch" and bifid ("split") scrotum with an undersized penis. This combination, referred to as pseudovaginal perineoscrotal hypospadias, is in the spectrum of ambiguous genitalia due to a number of conditions. Potential surgical problems: Scarring and contracture are occasional complications, but most unsatisfactory outcomes occur when a severe hypospadias needs to be repaired as well. Long-term complications can include fistulas between colon or upper rectum and skin or other cavities, or between urethra and perineum. Loss of sensation.

Cloacal repair is among the most complex of the surgeries described here. Bladder exstrophy or more severe cloacal exstrophy is a major birth defect involving inadequate closure and incomplete midline fusion of multiple pelvic and perineal organs as well as the front of the pelvis and lower abdominal wall. The penis and scrotum are often widely bifid (the two embryonic parts unjoined). The penis often cannot be salvaged, although the testes can be retained. Repair may involve closure of the bladder, closure of the anterior abdominal wall, colostomy (temporary or permanent) with reconstruction of the rectum. If the halves of the phallus cannot be joined, they may be removed. The smallest defect in this spectrum is an epispadias. Surgical repair for this is primarily a phalloplasty.[22] Potential surgical problems: Surgery for the more severe degrees of cloacal exstrophy is extensive and usually multistage. A variety of potential problems and complications can occur, including need for long-term colostomy or vesicostomy. In many cases a functional penis cannot be created. Scarring is often extensive and the lower torso severely disfigured even with fairly good outcomes.

Phalloplasty is a general term for any reconstruction of the penis itself, especially for more unusual types of injuries, deformities, or birth defects. The principal difficulty is that erectile tissue is not easily constructed and this limits the surgeon's ability to make more than minor size changes. Construction of a narrow tube lined with mucosa (a urethra) is a similar challenge. Potential surgical problems: Minor revisions of the skin are rarely followed by problems. More complicated reconstruction may result in scarring and contracture, which can distort the shape or curvature of the penis, or interfere with erections or make them painful.

Hysterectomy is removal of a uterus. It is rare that a uterus or Müllerian duct derivatives would need to be removed from a child being raised as a boy: see persistent Müllerian duct syndrome. The most common scenario is accidental discovery of persistent Müllerian derivatives or a small uterus during abdominal surgery of a normal boy for cryptorchidism, appendectomy, or bowel disease. Removal would not involve genital surgery. A rarer indication would be that of a completely virilized XX child with congenital adrenal hyperplasia (Prader stage 5) being raised as a male; ovaries and uterus must be removed to prevent breast development and menstruation by early adolescence. Potential surgical problems: Risks are simply those of abdominal surgery.

Testicular prostheses are saline-filled plastic ovoids implanted in the scrotum. They have no function except to provide the appearance and feel of testes. Several sizes are available, but most are implanted in adolescence to avoid repeated procedures to implant larger sizes at puberty. Prostheses made of silastic are no longer available due to safety and perception-of-safety concerns. Potential surgical problems: Foreign body reactions, rarely with infection or erosion of scrotal skin, are minimal but constitute the most significant complication.

Penile augmentation surgery is surgery intended to enlarge a small penis. Early attempts in the 1950s and 1960s involved constructing a tube of non-erectile flesh extending a small penis but the penis did not function. In recent years a small number of urologists have been offering an augmentation[clarification needed] procedure that involves moving outward some of the buried components of the corpora so that the penis protrudes more. The girth is augmented with transplantation of the patient's fat. This procedure is designed to preserve erectile and sexual function without surgically altering the urethra. This type of surgery is not performed on children and primarily produces a small increase in the size of a normal penis, but would be less likely to produce a major functional change in a severe micropenis. Potential surgical problems: Reabsorption of the fat is common. Scarring resulting in interference with erectile function is less likely but more damaging. Issues with physical sensation.

Concealed penis where a normal penis is buried in suprapubic fat. In most cases, when the fat is depressed with the fingers, the penis is seen to be of normal size. This is common in overweight boys before the penile growth of puberty. Surgical techniques have been devised to improve it.[23] Potential surgical problems: The most common difficulty is recurrence with further weight gain. Scarring can occur.

Feminizing surgical procedures[edit]

In the last 50 years, the following procedures were most commonly performed to make the genitalia more typically female: virilization due to congenital adrenal hyperplasia; genital variations due, for example, to cloacal exstrophy; genital variations in infants with XY or mixed chromosomes to be raised as girls, such as gonadal dysgenesis, partial and complete androgen insensitivity syndrome, micropenis, cloacal and bladder exstrophy. In the 21st-century, feminizing surgery to support reassignment of XY infants with non-ambiguous micropenis has been largely discontinued, and surgical reassignment of XY infants with exstrophy or other significant variations or injuries is diminishing. See history of intersex surgery.

Clitorectomy amputation or removal of most of the clitoris, including glans, erectile tissue, and nerves. This procedure was the most common clitoral surgery performed prior to 1970, but was largely abandoned by 1980 because it usually resulted in loss of clitoral sensation. Potential surgical problems: The primary effect of this surgery, not surprisingly, is a drastic reduction in ability to experience orgasm. The appearance is not very normal. Regrowth of unwanted erectile tissue has sometimes presented problems.

Clitoroplasty, like phalloplasty, is a term that encompasses any surgical reconstruction of the clitoris, such as removal of the corpora. Clitoral recession and reduction can both be referred to as clitoroplasty. Potential surgical problems: Major complications can include scarring, contractures, loss of sensation, loss of capacity for orgasm, and unsatisfactory appearance.

Clitoral recession involves the repositioning of the erectile body and glans of the clitoris farther back under the symphysis pubis and/or skin of the preputium and mons. This was commonly done from the 1970s through the 1980s to reduce protrusion without sacrificing sensation. Outcomes were often unsatisfactory, and it fell into disfavor in the last 15 years.[24] Potential surgical problems: Unfortunately the subsequent sensations were not always pleasant, and erection could be painful. Adults who had a clitoral recession in early childhood often report reduced capacity for enjoyment of sexual intercourse, though similar women who had not had surgery also report a high rate of sexual dysfunction.[25]

Clitoral reduction was developed in the 1980s to reduce size without reducing function. Lateral wedges of the erectile tissue of the clitoris are removed to reduce the size and protrusion. The neurovascular tissue is carefully spared to preserve function and sensation. Nerve stimulation and sensory responses are now often performed during the surgery to confirm function of the sensory nerves.[24][26] Clitoral reduction is rarely done except in combination with vaginoplasty when substantial virilization is present. Potential problems: The degree to which the goal of preserving sexual sensations is attained is a subject of controversy regarding the necessity of such treatments, and lack of firm evidence of good outcomes.[2][4] The success of more contemporary approaches was challenged by Thomas in 2004: "confidence in the superiority of modern surgery is almost certainly misplaced as the crucial components of current clitoral reduction surgery are not fundamentally different from those used in specialist centres 20 years ago".[27]

Vaginoplasty, the construction or reconstruction of a vagina, can be fairly simple or quite complex, depending on the initial anatomy. If a normal internal uterus, cervix and upper vagina (the Müllerian derivatives) exist, and the outer virilization is modest, surgery involves separating the fused labia and widening the vaginal introitus. With greater degrees of virilization, the major challenge of the procedure is to provide a passage connecting the outer vaginal opening to the cervix which will stay wide enough to allow coitus. XY girls or women with partial androgen insensitivity syndrome will have a blind vaginal pouch of varying degrees of depth. Sometimes this can be dilated to a usable depth. Sometimes surgery is performed to deepen it.

The most challenging surgery with the highest complication rate is construction of an entirely new vagina (a "neovagina"). The most common instance of this is when a child will be assigned and raised as a female despite complete virilization, as with Prader 5 CAH, or (in the past) when a genetic male infant with a severely defective penis was reassigned as a female. One method is to use a segment of colon, which provides a lubricated mucosal surface as a substitute for the vaginal mucosa. Another is to line the new vagina with a skin graft.[28][29][30] Potential surgical problems: Stenosis (narrowing) of the constructed vagina is the most common long-term complication and the chief reason that a revision may be required when a girl is older. When a neovagina is made from a segment of bowel, it tends to leak mucus; when made with a skin graft, lubrication is necessary. Less common complications include fistulas, uncomfortable scarring, and problems with urinary continence.[25][31][32]

Gonadectomy is removal of the gonads. If the gonads are dysgenetic testes or streak gonads and at least some of the cells have a Y chromosome, the gonads or streaks must be removed because they are nonfunctional but have a relatively high risk of developing gonadoblastoma. If the gonads are relatively "normal" testes, but the child is to be assigned and raised as female, (e.g., for intersex conditions with severe undervirilization, or major malformations involving an absent or unsalvageable penis) they must be removed before puberty to prevent virilization from rising testosterone.

Testes in androgen insensitivity are a special case: if there is any degree of responsiveness to testosterone, they should be removed before puberty. On the other hand, if androgen insensitivity is complete, the testes may be left to produce estradiol (via testosterone) to induce breast development, but there is a slowly increasing risk of cancer in adult life. Streak gonads without a Y chromosome cell line need not be removed but will not function. Finally, the gonads in true hermaphroditism must be directly examined; atypical gonads with Y line or potential testicular function should be removed but in rare instances a surgeon may try to preserve the ovarian part of an ovotestis.[33] Potential surgical problems: A lifetime of hormone replacement will be required, to avoid osteoporosis and enable sexual functioning.

Cloacal exstrophy and bladder exstrophy repair is needed regardless of the sex of assignment or rearing. Simple bladder exstrophy in a genetic female does not usually involve the vagina. Cloacal exstrophy in a genetic female usually requires major surgical reconstruction of the entire perineum, including bladder, clitoris, symphysis pubis, and both the vaginal introitus and urethra. However, the uterus and ovaries are normally formed. Severe bladder exstrophy or cloacal exstrophy in genetic males often renders the phallus widely split, small, and unsalvageable. The scrotum is also widely split, though testes themselves are usually normal. From the 1960s until the 1990s, many of these infants were assigned and raised as females, with fashioning of a vagina and gonadectomy as part of the perineal reconstruction.[22]

Potential surgical problems: Surgery for the more severe degrees of cloacal exstrophy is extensive and usually multistage. A variety of potential problems and complications can occur, including need for long-term colostomy or vesicostomy. Creating a functional urethra is difficult and poor healing, with scarring, stricture, or fistula can require a vesicostomy to prevent urinary incontinence. Construction of a functional internal and external anal sphincter can be equally difficult when this has been disrupted as well. Functional problems can warrant a temporary or long-term colostomy. The added challenge for the most severely affected genetic females, and for genetic males who are being raised as females, is construction of a neovagina. Scarring is extensive and the lower torso disfigured even with the best outcomes. Finally, it has become apparent that some XY males (without intersex conditions) who are reassigned and raised as females have not developed a female gender identity and have sought reassignment back to male.[34]

Hormone treatment[edit]

There is widespread evidence of prenatal testing and hormone treatment to prevent intersex traits.[35][36] In 1990, a paper by Heino Meyer-Bahlburg titled Will Prenatal Hormone Treatment Prevent Homosexuality? was published in the Journal of Child and Adolescent Psychopharmacology. It examined the use of "prenatal hormone screening or treatment for the prevention of homosexuality" using research conducted on foetuses with congenital adrenal hyperplasia (CAH). Dreger, Feder, and Tamar-Mattis describe how later research constructs "low interest in babies and men – and even interest in what they consider to be men's occupations and games – as "abnormal", and potentially preventable with prenatal dex[amethasone]".[35]

Genetic selection and terminations[edit]

The ethics of preimplantation genetic diagnosis to select against intersex traits was the subject of 11 papers in the October 2013 issue of the American Journal of Bioethics.[37] There is widespread evidence of pregnancy terminations arising from prenatal testing, as well prenatal hormone treatment to prevent intersex traits.

In April 2014, Organisation Intersex International Australia made a submission on genetic selection via Preimplantation genetic diagnosis to the National Health and Medical Research Council recommending that deselection of embryos and foetuses on grounds of intersex status should not be permitted. It quoted research by Professors Morgan Holmes, Jeff Nisker, associate professor Georgiann Davis, and by Jason Behrmann and Vardit Ravitsky.[38] It quotes research showing pregnancy termination rates of up to 88% in 47,XXY even while the World Health Organization describes the trait as "compatible with normal life expectancy", and "often undiagnosed".[39][40] Behrmann and Ravitsky find social concepts of sex, gender and sexual orientation to be "intertwined on many levels. Parental choice against intersex may thus conceal biases against same-sex attractedness and gender nonconformity."[41]

Gender dysphoria[edit]

The DSM-5 included a change from using Gender Identity Disorder to Gender Dysphoria. This revised code now specifically includes intersex people who do not identify with their sex assigned at birth, using the language of Disorders of Sex Development.[42] This move was criticised by intersex advocacy groups in Australia and New Zealand.[43]

Psychosocial support[edit]

A 2006 clinician "Consensus Statement on Intersex Disorders and Their Management" attempted to prioritise psychosocial support for children and families, but it also supports surgical intervention with psychosocial rationales such as "minimizing family concern and distress" and "mitigating the risks of stigmatization and gender-identity confusion".[44]

In 2012, the Swiss National Advisory Commission on Biomedical Ethics argued strongly in favour of improved psychosocial support, saying:[3]

The initial aim of counselling and support is therefore to create a protected space for parents and the newborn, so as to facilitate a close bond. In addition, the parents need to be enabled to take the necessary decisions on the child's behalf calmly and after due reflection. In this process, they should not be subjected to time or social pressures. Parents' rapid requests for medical advice or for corrective surgery are often a result of initial feelings of helplessness, which need to be overcome so as to permit carefully considered decision-making.

It is important to bear in mind and also to point out to the parents that a diagnosis does not in itself entail any treatment or other medical measures, but serves initially to provide an overview of the situation and a basis for subsequent decisions, which may also take the form of watchful waiting.

...interventions have lasting effects on the development of identity, fertility, sexual functioning and the parent-child relationship. The parents' decisions should therefore be marked by authenticity, clarity and full awareness, and based on love for the child, so that they can subsequently be openly justified vis-à-vis the child or young adult.

A joint international statement by intersex community organizations published in 2013 sought, amongst other demands:

Recognition that medicalization and stigmatisation of intersex people result in significant trauma and mental health concerns.

In view of ensuring the bodily integrity and well-being of intersex people, autonomous non-pathologising psycho-social and peer support be available to intersex people throughout their life (as self-required), as well as to parents and/or care providers.

Outcomes and evidence[edit]

Specialists at the Intersex Clinic at University College London began to publish evidence in 2001 that indicated the harm that can arise as a result of inappropriate interventions, and advised minimising the use of childhood surgical procedures.[45][46][47][48][49][50][51][52][49][53]

A 2004 paper by Heino Meyer-Bahlburg and others examined outcomes from early surgeries in individuals with XY variations, at one patient centre.[54] The study has been used to support claims that "‘the majority of women...have clearly favored genital surgery at an earlier age" but the study was criticized by Baratz and Feder in a 2015 paper for neglecting to inform respondents that:

"(1) not having surgery at all might be an option; (2) they might have had lower rates of reoperation for stenosis if surgery were performed later, or (3) that significant technical improvements that were expected to improve outcomes had occurred in the 13 or 14 years between when they underwent early childhood surgery and when it might have been deferred until after puberty".[55]

Chicago consensus statement[edit]

In 2006, an invited group of clinicians met in Chicago and reviewed clinical evidence and protocols, and adopted a new term for intersex conditions: Disorders of sex development (DSD) in the journal article Consensus Statement on Intersex Disorders and their Management.[44] The new term refers to "congenital conditions in which development of chromosomal, gonadal, or anatomical sex is atypical."[44] The term has been controversial and not widely adopted outside clinical settings: the World Health Organization and many medical journals still refer to intersex traits or conditions.[56] Academics like Georgiann Davis and Morgan Holmes, and clinical psychologists like Tiger Devore argue that the term DSD was designed to "reinstitutionalise" medical authority over intersex bodies.[4][57][58][59] On surgical rationales and outcomes, the article stated that:

It is generally felt that surgery that is carried out for cosmetic reasons in the first year of life relieves parental distress and improves attachment between the child and the parents. The systematic evidence for this belief is lacking. ... information across a range of assessments is insufficient ... outcomes from clitoroplasty identify problems related to decreased sexual sensitivity, loss of clitoral tissue, and cosmetic issues ... Feminising as opposed to masculinising genitoplasty requires less surgery to achieve an acceptable outcome and results in fewer urological difficulties... Long term data on sexual function and quality of life among those assigned female as well as male show great variability. There are no controlled clinical trials of the efficacy of early (less than 12 months of age) versus late surgery (in adolescence and adulthood), or of the efficacy of different techniques"[44]

Changing practices?[edit]

Data presented in recent years suggests that little has changed in practice.[60] Creighton and others in the UK have found that there have been few audits of the implementation of the 2006 statement, clitoral surgeries on under-14s have increased since 2006, and "recent publications in the medical literature tend to focus on surgical techniques with no reports on patient experiences".[12]

Patient outcomes[edit]

A 2014 civil society submission to the World Health Organization cited data from a large German Netzwerk DSD/Intersexualität study:

In a study in Lübeck conducted between 2005 and 2007 ... 81% of 439 individuals had been subjected to surgeries due to their intersex diagnoses. Almost 50% of participants reported psychological problems. Two thirds of the adult participants drew a connection between sexual problems and their history of surgical treatment. Participating children reported significant disturbances, especially within family life and physical well-being – these are areas that the medical and surgical treatment was supposed to stabilize.[13]

A 2016 Australian study of persons born with atypical sex characteristics found that "strong evidence suggesting a pattern of institutionalised shaming and coercive treatment of people". Large majorities of respondents opposed standard clinical protocols.[61]

2016 Global DSD Update[edit]

A 2016 follow-up to the 2006 Consensus Statement, termed a Global Disorders of Sex Development Update stated,

There is still no consensual attitude regarding indications, timing, procedure and evaluation of outcome of DSD surgery. The levels of evidence of responses given by the experts are low (B and C), while most are supported by team expertise... Timing, choice of the individual and irreversibility of surgical procedures are sources of concerns. There is no evidence regarding the impact of surgically treated or non-treated DSDs during childhood for the individual, the parents, society or the risk of stigmatization... Physicians working with these families should be aware that the trend in recent years has been for legal and human rights bodies to increasingly emphasize preserving patient autonomy.[10]

A 2016 paper on "Surgery in disorders of sex development (DSD) with a gender issue" repeated many of the same claims, but without reference to human rights norms.[11] A commentary to that article by Alice Dreger and Ellen Feder criticized that omission, stating that issues have barely changed in two decades, with "lack of novel developments", while "lack of evidence appears not to have had much impact on physicians’ confidence in a standard of care that has remained largely unchanged."[62] Another 2016 commentary stated that the purpose of the 2006 Consensus Statement was to validate existing practices, "The authoritativeness and "consensus" in the Chicago statement lies not in comprehensive clinician input or meaningful community input, but in its utility to justify any and all forms of clinical intervention."[63]

Controversies and unsettled questions[edit]

Management practices for intersex conditions have evolved over the last 60 years. In recent decades surgical practices have become the subject of public and professional controversy, and evidence remains lacking.[10][11]

Comparing early against late surgeries[edit]

Argued or putative advantages of infant surgery:

  • Tissue is more elastic and heals better according to many surgeons.
  • Genital surgery performed before the age of memory is less emotionally traumatic.
  • Surgery in infancy avoids asking adolescent to make a decision that is stressful and difficult even for adults.
  • Assuming infant surgery is successful, there is no barrier to engaging in normal sexual activities, and less distortion of psychosexual identity.

Argued or putative advantages of surgery in adolescence or later:

  • If outcome is less than satisfactory, early surgery leaves a person wondering if she would have been better off without it.
  • Any surgery not absolutely necessary for physical health should be postponed until the person is old enough to give informed consent.
  • Genital surgery should be handled differently than other birth defect surgery; this is a type of surgery that parents should not be empowered to make decisions about because they will be under social pressure to make "bad" decisions.
  • By mid-adolescence or later, persons may decide that their atypical genitalia do not need to be changed.
  • Infant vaginoplasties should not be done because most women who have had them performed report some degree of difficulty with sexual function; even though we have no evidence that adult sexual function will be better if surgery is deferred, the outcomes couldn't be worse than they currently are after infant surgery.

Others argue that the key questions are not ones of early or late surgery, but questions of consent and autonomy.[63][64]

Parental consent[edit]

Parents are frequently considered able to consent to feminizing or masculinizing interventions on their child, and this may be considered standard for the treatment of physical disorders. However this is contested, particularly where interventions seek to address psychosocial concerns. A BMJ editorial in 2015 stated that parents are unduly influenced by medicalized information, may not realize that they are consenting to experimental treatments, and regret may be high.[18] Research has suggested that parents are willing to consent to appearance-altering surgeries even at the cost of later adult sexual sensation.[65] Child rights expert Kirsten Sandberg states that parents have no right to consent to such treatments.[66]

Sensation and sexual function[edit]

Reports published in the early 1990s state that 20-50% of surgical cases result in a loss of sexual sensation.[67][68]

A 2007 paper by Yang, Felsen and Poppas provided what the authors believe is the first study of clitoral sensitivity after clitoris reduction surgery, but the research was itself the subject of ethical debate. Postoperative patients aged over than 5-years were "considered candidates" for clitoral sensitivity testing, and 10 of 51 patients were tested, with 9 undergoing extended vibratory sensory testing. The initial tests were performed on the inner thigh, labia majora, labia minora, vaginal introitus and clitoris, with a "cotton tip applicator" and extended tests with a biothesiometer, a medical device used to measure sensitivity thresholds. Values were recorded. The authors note that there are no control data "for assessment of the viability and function of the clitoris in unaffected women."[69] The ethics of these tests have been criticized by bioethicists,[70] and subsequently defended by the Office for Human Research Protections.[71]

Loss of sexual function and sensation remains a concern in a submission by the Australasian Paediatric Endocrine Group to the Australian Senate in 2013.[2] Clinical decision-making has prioritized perceived advantages from infant clitoral reduction surgery over the potential disadvantages of reduced or distorted sexual sensation. Human rights institutions stress the informed consent of the individual concerned.

Decision-making on cancer and other physical risks[edit]

In the cases where nonfunctional testes are present, or with partial androgen insensitivity syndrome, there is a risk that these develop cancer. They are removed by orchidectomy or monitored carefully.[72] In a major Parliamentary report in Australia, published in October 2013, the Senate Community Affairs References committee was "disturbed" by the possible implications of current practices in the treatment of cancer risk. The committee stated: "clinical intervention pathways stated to be based on probabilities of cancer risk may be encapsulating treatment decisions based on other factors, such as the desire to conduct normalising surgery… Treating cancer may be regarded as unambiguously therapeutic treatment, while normalising surgery may not. Thus basing a decision on cancer risk might avoid the need for court oversight in a way that a decision based on other factors might not. The committee is disturbed by the possible implications of this..."[4]

Gender identity issues[edit]

Gender identity and sexuality in intersex children have been problematized, and subjective judgements are made about the acceptability of risk of future gender dysphoria[11][73] Medical professionals have traditionally considered the worst outcomes after genital reconstruction in infancy to occur when the person develops a gender identity discordant with the sex assigned as an infant. Most of the cases in which a child or adult has voluntarily changed sex and rejected sex of assignment and rearing have occurred in partially or completely virilized genetic males who were reassigned and raised as females. This is the management practice that has been most thoroughly undermined in recent decades, as a result of a small number of spontaneous self-reassignments to male. Reducing the likelihood of a gender "mismatch" is also a claimed advantage of deferring reconstructive surgery until the patient is old enough to assess gender identity with confidence.

Human rights institutions question such approaches as being "informed by redundant social constructs around gender and biology"[74]

Stigma and normality[edit]

Parents may be advised that without surgery, their child will be stigmatized,[75] but they may make different choices with non-medicalized information.[76] However, there is no evidence that surgeries help children grow up psychologically "normal".[10][77]

Unlike other aesthetic surgical procedures performed on infants, such as corrective surgery for a cleft lip (as opposed to a cleft palate), genital surgery may lead to negative consequences for sexual functioning in later life (such as loss of sensation in the genitals, for example, when a clitoris deemed too large or penis is reduced/removed), or feelings of freakishness and unacceptability, which may have been avoided without the surgery. Studies have revealed how surgical intervention has had psychological effects, impacting on well-being and quality of life. Genital surgeries do not ensure a successful psychological outcome for the patient and might require psychological support when the patient is trying to distinguish a gender identity.[78] The Swiss National Advisory Commission on Biomedical Ethics states that, where "interventions are performed solely with a view to integration of the child into a family and social environment, then they run counter to the child's welfare. In addition, there is no guarantee that the intended purpose (integration) will be achieved."[3]

Opponents of all "corrective surgery" on atypical sex characteristics suggest to change social opinion regarding the desirability of having genitalia that look more average, rather than perform surgery to try to make them more like those of other people.

Medical photography and display[edit]

Photographs of intersex children's genitalia are circulated in medical communities for documentary purposes, and individuals with intersex traits may be subjected to repeated genital examinations and display to medical teams. Problems associated with experiences of medical photography of intersex children have been discussed[79] along with their ethics, control and usage.[80] "The experience of being photographed has exemplified for many people with intersex conditions the powerlessness and humiliation felt during medical investigations and interventions".[80]

Secrecy and information provision[edit]

Additionally, parents are not often consulted on the decision-making process when choosing the sex of the child, and they may be advised to conceal information from their child. The Intersex Society of North America stated that "For decades, doctors have thought it necessary to treat intersex with a concealment-centered approach, one that features downplaying intersex as much as possible, even to the point of lying to patients about their conditions."[81]

Alternative pathways[edit]

In 2015, an editorial in the British Medical Journal (BMJ) described current surgical interventions as experimental, stating that clinical confidence in constructing "normal" genital anatomies has not been borne out, and that medically credible pathways other than surgery do not yet exist.[18]

Human rights issues[edit]

Protection of intersex children from harmful practices
  Legal prohibition of non-consensual medical interventions
  Regulatory suspension of non-consensual medical interventions

The Council of Europe highlights several areas of concern in relation to intersex surgeries and other medical treatment:

  • unnecessary "normalising" treatment of intersex persons, and unnecessary pathologisation of variations in sex characteristics.
  • access to justice and reparation for unnecessary medical treatment, as well as inclusion in equal treatment and hate crime law.
  • access to information, medical records, peer and other counselling and support.
  • respecting self-determination in gender recognition, through expeditious access to official documents.[3][4][6]

The Council of Europe argues that secrecy and shame have perpetuated human rights abuses and a lack of social understanding of the reality of intersex people. It calls for respect for "intersex persons' right not to undergo sex assignment treatment".[6]

Alice Dreger, a US professor of Clinical Medical Humanities and Bioethics, argues that little has changed in actual clinical practice in recent years.[60] Creighton and others in the UK have found that there have been few audits of the implementation of the 2006 statement, clitoral surgeries on under-14s have increased since 2006, and "recent publications in the medical literature tend to focus on surgical techniques with no reports on patient experiences".[12]

Institutions like the Swiss National Advisory Commission on Biomedical Ethics,[3] the Australian Senate,[4] the Council of Europe,[6][82] World Health Organisation,[1][83] and UN Office of the High Commissioner for Human Rights[84] and Special Rapporteur on Torture[14] have all published reports calling for changes to clinical practice.

In 2011, Christiane Völling won the first successful case brought against a surgeon for non-consensual surgical intervention. The Regional Court of Cologne, Germany, awarded her €100,000.[5]

In April 2015, Malta became the first country to recognize a right to bodily integrity and physical autonomy, and outlaw non-consensual modifications to sex characteristics. The Act was widely welcomed by civil society organizations.[7][8][9][85]

See also[edit]

Notes[edit]

  1. ^ a b c World Health Organization (2015). Sexual health, human rights and the law. Geneva: World Health Organization. ISBN 9789241564984. 
  2. ^ a b c Submission 88 to the Australian Senate inquiry on the involuntary or coerced sterilisation of people with disabilities in Australia, Australasian Paediatric Endocrine Group (APEG), 27 June 2013
  3. ^ a b c d e f Swiss National Advisory Commission on Biomedical Ethics NEK-CNE (November 2012). On the management of differences of sex development. Ethical issues relating to "intersexuality".Opinion No. 20/2012 (PDF). 2012. Berne. 
  4. ^ a b c d e f Australian Senate; Community Affairs References Committee (October 2013). Involuntary or coerced sterilisation of intersex people in Australia. Canberra: Community Affairs References Committee. ISBN 9781742299174. 
  5. ^ a b Zwischengeschlecht (December 17, 2015). "Nuremberg Hermaphrodite Lawsuit: Michaela "Micha" Raab Wins Damages and Compensation for Intersex Genital Mutilations!" (text). Retrieved 2015-12-21. 
  6. ^ a b c d e Council of Europe; Commissioner for Human Rights (April 2015), Human rights and intersex people, Issue Paper 
  7. ^ a b Cabral, Mauro (April 8, 2015). "Making depathologization a matter of law. A comment from GATE on the Maltese Act on Gender Identity, Gender Expression and Sex Characteristics". Global Action for Trans Equality. Retrieved 2015-07-03. 
  8. ^ a b OII Europe (April 1, 2015). "OII-Europe applauds Malta's Gender Identity, Gender Expression and Sex Characteristics Act. This is a landmark case for intersex rights within European law reform". Retrieved 2015-07-03. 
  9. ^ a b Reuters (1 April 2015). "Surgery and Sterilization Scrapped in Malta's Benchmark LGBTI Law". The New York Times. 
  10. ^ a b c d Lee, Peter A.; Nordenström, Anna; Houk, Christopher P.; Ahmed, S. Faisal; Auchus, Richard; Baratz, Arlene; Baratz Dalke, Katharine; Liao, Lih-Mei; Lin-Su, Karen; Looijenga, Leendert H.J.; Mazur, Tom; Meyer-Bahlburg, Heino F.L.; Mouriquand, Pierre; Quigley, Charmian A.; Sandberg, David E.; Vilain, Eric; Witchel, Selma; and the Global DSD Update Consortium (2016-01-28). "Global Disorders of Sex Development Update since 2006: Perceptions, Approach and Care". Hormone Research in Paediatrics. 85 (3): 158–180. ISSN 1663-2818. doi:10.1159/000442975. Retrieved 2016-01-30. 
  11. ^ a b c d Mouriquand, Pierre D. E.; Gorduza, Daniela Brindusa; Gay, Claire-Lise; Meyer-Bahlburg, Heino F. L.; Baker, Linda; Baskin, Laurence S.; Bouvattier, Claire; Braga, Luis H.; Caldamone, Anthony C.; Duranteau, Lise; El Ghoneimi, Alaa; Hensle, Terry W.; Hoebeke, Piet; Kaefer, Martin; Kalfa, Nicolas; Kolon, Thomas F.; Manzoni, Gianantonio; Mure, Pierre-Yves; Nordenskjöld, Agneta; Pippi Salle, J. L.; Poppas, Dix Phillip; Ransley, Philip G.; Rink, Richard C.; Rodrigo, Romao; Sann, Léon; Schober, Justine; Sibai, Hisham; Wisniewski, Amy; Wolffenbuttel, Katja P.; Lee, Peter. "Surgery in disorders of sex development (DSD) with a gender issue: If (why), when, and how?". Journal of Pediatric Urology. 12: 139–149. ISSN 1477-5131. doi:10.1016/j.jpurol.2016.04.001. Retrieved 2016-05-30. 
  12. ^ a b c Creighton, Sarah M.; Michala, Lina; Mushtaq, Imran; Yaron, Michal (January 2, 2014). "Childhood surgery for ambiguous genitalia: glimpses of practice changes or more of the same?". Psychology and Sexuality. 5 (1): 34–43. ISSN 1941-9899. doi:10.1080/19419899.2013.831214. Retrieved 2015-07-19. 
  13. ^ a b Intersex Issues in the International Classification of Diseases: a revision (PDF). Mauro Cabral, Morgan Carpenter (eds.). 2014. 
  14. ^ a b Report of the UN Special Rapporteur on Torture, Office of the UN High Commissioner for Human Rights, February 2013.
  15. ^ Asia Pacific Forum of National Human Rights Institutions (June 2016). Promoting and Protecting Human Rights in relation to Sexual Orientation, Gender Identity and Sex Characteristics. Asia Pacific Forum of National Human Rights Institutions. ISBN 978-0-9942513-7-4. 
  16. ^ Comisión Interamericana de Derechos Humanos (2015-11-12), Violencia contra Personas Lesbianas, Gays, Bisexuales, Trans e Intersex en América (PDF), Comisión Interamericana de Derechos Humanos 
  17. ^ German Ethics Council (February 2012). Intersexuality, Opinion. ISBN 978-3-941957-50-3. 
  18. ^ a b c Liao, Lih-Mei; Wood, Dan; Creighton, Sarah M (28 September 2015). "Parental choice on normalising cosmetic genital surgery". The BMJ: –5124. ISSN 1756-1833. doi:10.1136/bmj.h5124. Retrieved 30 September 2015. 
  19. ^ Glassberg, KI (1999). "Editorial: gender assignment and the pediatric urologist". J Urol. 161: 1308–10. doi:10.1016/s0022-5347(01)61676-8. 
  20. ^ Barbagli, Guido; Sansalone, Salvatore; Djinovic, Rados; Lazzeri, Massimo (2012). "Surgical Repair of Late Complications in Patients Having Undergone Primary Hypospadias Repair during Childhood: A New Perspective". Advances in Urology. 2012: 1–5. ISSN 1687-6369. doi:10.1155/2012/705212. Retrieved 2015-07-19. 
  21. ^ Carmack, Adrienne; Notini, Lauren; Earp, Brian (2015). "Should Surgery for Hypospadias Be Performed Before an Age of Consent?". Journal of Sex Research. in press: 1–12. doi:10.1080/00224499.2015.1066745. 
  22. ^ a b Schober JM, Carmichael PA, Hines M, Ransley PG (2002). "The ultimate challenge of cloacal exstrophy". J Urol. 167: 300–4. doi:10.1016/s0022-5347(05)65455-9. 
  23. ^ Casale AJ, Beck SD, Cain MP, Adams MC, Rink RC (1999). "Concealed penis in childhood: a spectrum of etiology and treatment". J Urol. 162: 1165–8. doi:10.1016/s0022-5347(01)68114-x. 
  24. ^ a b Rangecroft L, Brain C, Creighton S, Di Ceglie D, Ogilvy-Stuart A, Malone P, Turnock R. [1] Statement of the British Association of Pediatric Surgeons Working Party on the Surgical Management of Children Born with Ambiguous Genitalia. July 2001.
  25. ^ a b Minto CL, Liao LM, Woodhouse CR, Ransley PG, Creighton SM (2003). "The effect of clitoral surgery on sexual outcome in individuals who have intersex conditions with ambiguous genitalia: a cross-sectional study". Lancet. 361: 1252–7. PMID 12699952. doi:10.1016/s0140-6736(03)12980-7. 
  26. ^ Chase, C (1996). "Re: Measurement of pudendal evoked potentials during feminizing genitoplasty: technique and applications (letter)". J Urol. 156: 1139–40. doi:10.1016/s0022-5347(01)65736-7. 
  27. ^ Thomas, D F M (2004). "Gender assignment: background and current controversies". BJU International. 93, Supplement 3: 47–50. 
  28. ^ Creighton S (2001). "Surgery for intersex". J Royal Soc Med. 94: 218–20. 
  29. ^ Rink RC, Adams MC (1998). "Feminizing genitoplasty: state of the art". World J Urol. 16: 212–218. doi:10.1007/s003450050055. 
  30. ^ Schnitzer JJ, Donahoe PK (2001). "Surgical treatment of congenital adrenal hyperplasia". Endocrinol Metab Clin N Am. 30: 137–54. doi:10.1016/s0889-8529(08)70023-9. 
  31. ^ Alizai NK, Thomas DF, Lilford RJ, Batchelor AG, Johnson N (1999). "Feminizing genitoplasty for congenital adrenal hyperplasia: what happens at puberty?". J Urol. 161: 1588–91. PMID 10210421. doi:10.1016/s0022-5347(05)68986-0. 
  32. ^ Lobe TE, Woodall DL, Richards GE, Cavallo A, Meyer WJ (1987). "The complications of surgery for intersex: changing patterns over two decades". J Pediatr Surg. 22: 651–2. PMID 3612461. doi:10.1016/s0022-3468(87)80119-7. 
  33. ^ Manuel M, Katayama PK, Jones HW. "Jr. 1976 The age of occurrence of gonadal tumors in intersex patients with a Y chromosome". Am J Obstet Gynecol. 124: 293–300. 
  34. ^ Reiner WG, Gearhart JP (2004). "Discordant sexual identity in some genetic males with cloacal exstrophy assigned to female sex after birth". New Engl J Med. 350: 333–41. doi:10.1056/nejmoa022236. 
  35. ^ a b Bioethics Forum blog – Preventing Homosexuality (and Uppity Women) in the Womb?, Alice Dreger, Ellen K. Feder, Anne Tamar-Mattis (2010), at Hastings Center Bioethics Blog, retrieved 18 May 2012.
  36. ^ Meyer-Bahlburg, H. F. L. (1 June 1999). "What Causes Low Rates of Child-Bearing in Congenital Adrenal Hyperplasia?". The Journal of Clinical Endocrinology & Metabolism. 84 (6): 1844–1847. doi:10.1210/jcem.84.6.5718. Retrieved 18 May 2012. 
  37. ^ "American Journal of Bioethics, 13:10, 51-53. Retrieved 11 September 2013". Retrieved 6 October 2014. 
  38. ^ Submission on the ethics of genetic selection against intersex traits, Organisation Intersex International Australia, 29 April 2014.
  39. ^ A. F. Radicioni, A. Ferlin, G. Balercia, D. Pasquali, L. Vignozzi, M. Maggi, C. Foresta, A. Lenzi (2010) Consensus statement on diagnosis and clinical management of Klinefelter syndrome, in Journal of Endocrinological Investigation, December 2010, Volume 33, Issue 11, pp 839-850.
  40. ^ Gender and Genetics, World Health Organization Genomic resource centre, undated, retrieved 22 April 2014.
  41. ^ Queer Liberation, Not Elimination: Why Selecting Against Intersex is Not "Straight" Forward, Jason Behrmann and Vardit Ravitsky (2013) in the American Journal of Bioethics, 13:10, 51-53. Retrieved 11 September 2013.
  42. ^ Kraus, Cynthia (May 2015). "Classifying Intersex in DSM-5: Critical Reflections on Gender Dysphoria". Archives of Sexual Behavior. 44 (5): 1147–1163. ISSN 0004-0002. PMID 25944182. doi:10.1007/s10508-015-0550-0. Retrieved 19 July 2015. 
  43. ^ "OII Australia and OII Aotearoa submission on the DSM-5 and SOC-7". Organisation Intersex International Australia. Retrieved 6 October 2014. 
  44. ^ a b c d Lee P. A., Houk C. P., Ahmed S. F., Hughes I. A.; Houk; Ahmed; Hughes (2006). "Consensus statement on management of intersex disorders". Pediatrics. 118 (2): e488–500. PMID 16882788. doi:10.1542/peds.2006-0738. 
  45. ^ Creighton, Sarah M.; Minto, Catherine L.; Steele, Stuart J. (July 14, 2001). "Objective cosmetic and anatomical outcomes at adolescence of feminising surgery for ambiguous genitalia done in childhood". The Lancet. 358: 124–125. PMID 11463417. doi:10.1016/s0140-6736(01)05343-0. 
  46. ^ Creighton, Sarah M (2001). "Editorial: Surgery for Intersex". Journal of the Royal Society of Medicine. 94 (5): 218–220. 
  47. ^ Minto, Catherine L.; Creighton, Sarah; Mrcog, Md; Woodhouse, Christopher (August 1, 2001). "Long term sexual function in intersex conditions with ambiguous genitalia". Journal of Pediatric and Adolescent Gynecology. 14 (3): 141–142. ISSN 1083-3188. doi:10.1016/S1083-3188(01)00111-5. 
  48. ^ Creighton, Sarah; Minto, Catherine L.; Steele, Stuart J. (August 1, 2001). "Cosmetic and anatomical outcomes following feminising childhood surgery for intersex conditions". Journal of Pediatric and Adolescent Gynecology. 14 (3): 142. ISSN 1083-3188. doi:10.1016/S1083-3188(01)00112-7. 
  49. ^ a b Minto, Catherine L; Liao, K.Lih-Mei; Conway, Gerard S; Creighton, Sarah M (July 2003). "Sexual function in women with complete androgen insensitivity syndrome". Fertility and Sterility. 80 (1): 157–164. ISSN 0015-0282. PMID 12849818. doi:10.1016/S0015-0282(03)00501-6. 
  50. ^ Creighton, Sarah; Minto, Catherine (December 2001). "Managing intersex, Most vaginal surgery in childhood should be deferred". British Medical Journal. 323: 1264–1265. PMC 1121738Freely accessible. PMID 11731376. doi:10.1136/bmj.323.7324.1264. 
  51. ^ Minto, Catherine L; Liao, Lih-Mei; Woodhouse, Christopher R. J.; Ransley, Phillip; Creighton, Sarah M (April 12, 2003). "The effect of clitoral surgery on sexual outcome in individuals who have intersex conditions with ambiguous genitalia: a cross-sectional study". The Lancet. 361: 1252–1257. PMID 12699952. doi:10.1016/s0140-6736(03)12980-7. 
  52. ^ Creighton, Sarah; Ransley, Philip; Duffy, Patrick; Wilcox, Duncan; Mushtaq, Imran; Cuckow, Peter; Woodhouse, Christopher; Minto, Catherine; Crouch, Naomi; Stanhope, Richard; Hughes, Ieuan; Dattani, Mehul; Hindmarsh, Peter; Brain, Caroline; Achermann, John; Conway, Gerard; Liao, Lih Mei; Barnicoat, Angela; Perry, Les (July 2003). "Regarding the Consensus Statement on 21-Hydroxylase Deficiency from the Lawson Wilkins Pediatric Endocrine Society and The European Society for Paediatric Endocrinology". The Journal of Clinical Endocrinology & Metabolism. 88 (7): 3454–3456. ISSN 0021-972X. doi:10.1210/jc.2003-030127. 
  53. ^ Crouch, Naomi S.; Minto, Catherine L.; Liao, Lih-Mei; Woodhouse, C R J; Creighton, Sarah M. (2004). "Genital sensation after feminizing genitoplasty for congenital adrenal hyperplasia: a pilot study". BJU International. 93: 135–138. doi:10.1046/j.1464-410X.2004.04572.x. 
  54. ^ Meyer-Bahlburg, H.F.L.; Migeon, C.J.; Berkovitz, G.D.; Gearhart, J.P.; Dolezal, C.; Wisniewski, A.B. (2004). "Attitudes of Adult 46,XY Intersex Persons to Clinical Management Policies". The Journal of Urology. 171 (4): 1615–1619. ISSN 0022-5347. PMID 15017234. doi:10.1097/01.ju.0000117761.94734.b7. Retrieved 2016-08-29. 
  55. ^ Baratz, Arlene B.; Feder, Ellen K. (2015). "Misrepresentation of Evidence Favoring Early Normalizing Surgery for Atypical Sex Anatomies". Archives of Sexual Behavior. 44: 1761–1763. ISSN 0004-0002. doi:10.1007/s10508-015-0529-x. Retrieved 2016-08-29. 
  56. ^ Rebecca Jordan-Young, Peter Sonksen, Katrina Karkazis (2014). "Sex, health, and athletes". BMJ. 348: g2926. PMID 24776640. doi:10.1136/bmj.g2926. 
  57. ^ An Interview with Dr. Tiger Howard Devore PhD, We Who Feel Differently, February 7, 2011.
  58. ^ Georgiann Davis (2011), "DSD is a Perfectly Fine Term": Reasserting Medical Authority through a Shift in Intersex Terminology, in PJ McGann, David J. Hutson (ed.) Sociology of Diagnosis (Advances in Medical Sociology, Volume 12), Emerald Group Publishing Limited, pp.155-182
  59. ^ Holmes, Morgan (2011). "The Intersex Enchiridion: Naming and Knowledge in the Clinic". Somatechnics. 1 (2): 87–114. doi:10.3366/soma.2011.0026. 
  60. ^ a b Dreger, Alice (April 3, 2015). "Malta Bans Surgery on Intersex Children". The Stranger SLOG. 
  61. ^ Jones, Tiffany; Hart, Bonnie; Carpenter, Morgan; Ansara, Gavi; Leonard, William; Lucke, Jayne (2016). Intersex: Stories and Statistics from Australia (PDF). Cambridge, UK: Open Book Publishers. ISBN 978-1-78374-208-0. Retrieved 2016-08-29. 
  62. ^ Feder, Ellen K.; Dreger, Alice (May 2016). "Still ignoring human rights in intersex care". Journal of Pediatric Urology. ISSN 1477-5131. doi:10.1016/j.jpurol.2016.05.017. Retrieved 2016-09-05. 
  63. ^ a b Carpenter, Morgan (May 2016). "The human rights of intersex people: addressing harmful practices and rhetoric of change". Reproductive Health Matters. 24 (47): 74–84. ISSN 0968-8080. doi:10.1016/j.rhm.2016.06.003. Retrieved 2016-09-05. 
  64. ^ Tamar-Mattis, A. (August 2014). "Patient advocate responds to DSD surgery debate". Journal of Pediatric Urology. 10 (4): 788–789. ISSN 1477-5131. PMID 24909610. doi:10.1016/j.jpurol.2014.03.019. 
  65. ^ Dayner, Jennifer E.; Lee, Peter A.; Houk, Christopher P. (October 2004). "Medical Treatment of Intersex: Parental Perspectives". The Journal of Urology. 172 (4): 1762–1765. ISSN 0022-5347. doi:10.1097/01.ju.0000138519.12573.3a. 
  66. ^ Sandberg, Kirsten (October 2015). "The Rights of LGBTI Children under the Convention on the Rights of the Child". Nordic Journal of Human Rights. 33 (4): 337–352. ISSN 1891-8131. doi:10.1080/18918131.2015.1128701. 
  67. ^ Newman, Kurt; et al. (1992). "Functional Results in Women Having Clitoral Reduction as Infants". Journal of Pediatric Surgery. 27 (2): 180–4. doi:10.1016/0022-3468(92)90308-t. 
  68. ^ Newman, Kurt; et al. (1991). "The Surgical Management of Infants and Children with Ambiguous Genitalia: Lessons learned from 25 years". Annals of Surgery. 215 (6): 644–53. doi:10.1097/00000658-199206000-00011. 
  69. ^ Yang, Jennifer; Felsen, Diane; Poppas, Dix P. (October 2007). "Nerve Sparing Ventral Clitoroplasty: Analysis of Clitoral Sensitivity and Viability". The Journal of Urology. 178 (4): 1598–1601. ISSN 0022-5347. doi:10.1016/j.juro.2007.05.097. 
  70. ^ Dreger, Alice; Feder, Ellen K (June 16, 2010). "Bad Vibrations". Hastings Center Bioethics Forum Blog. 
  71. ^ Dreger, Alice Domurat (2015). Galileo's Middle Finger: heretics, activists, and the search for justice in science. New York: Penguin Press. ISBN 9781594206085. 
  72. ^ Cools, Martine; Koen van Aerde, Anne-Marie Kersemaekers, Marjan Boter, Stenvert L. S. Drop, Katja P. Wolffenbuttel, Ewout W. Steyerberg, J. Wolter Oosterhuis, Leendert H. J. Looijenga (September 2005). "Morphological and Immunohistochemical Differences between Gonadal Maturation Delay and Early Germ Cell Neoplasia in Patients with Undervirilization Syndromes". J. Clin. Endo. 90 (9): 5295–5303. doi:10.1210/jc.2005-0139. Retrieved 18 June 2012. 
  73. ^ Furtado P. S.; et al. (2012). "Gender dysphoria associated with disorders of sex development". Nat. Rev. Urol. 9 (11): 620–627. PMID 23045263. doi:10.1038/nrurol.2012.182. 
  74. ^ Australian Human Rights Commission (June 2015). Resilient Individuals: Sexual Orientation, Gender Identity & Intersex Rights. Sydney: Australian Human Rights Commission. ISBN 978-1-921449-71-0. 
  75. ^ Morgan Holmes (2002). Rethinking the Meaning and Management of Intersexuality. Sexualities, 159–180."
  76. ^ Streuli, Jürg C.; Vayena, Effy; Cavicchia-Balmer, Yvonne; Huber, Johannes (August 2013). "Shaping Parents: Impact of Contrasting Professional Counseling on Parents' Decision Making for Children with Disorders of Sex Development". The Journal of Sexual Medicine. 10 (8): 1953–1960. ISSN 1743-6095. doi:10.1111/jsm.12214. 
  77. ^ Intersex Society of North America (24 May 2006). "What evidence is there that you can grow up psychologically healthy with intersex genitals (without "normalizing" surgeries)?". Retrieved 25 November 2006. 
  78. ^ Bean, E. J.; Mazur, T.; Robinson, A. D. (2009). "Mayer-Rokitansky-Küster-Hauser Syndrome: Sexuality, Psychological Effects, and Quality of Life". Journal of Pediatric and Adolescent Gynecology. 22 (6): 339–346. PMID 19589707. doi:10.1016/j.jpag.2008.11.006. 
  79. ^ Preves, Sharon (2003). Intersex and Identity, the Contested Self. Rutgers. ISBN 0-8135-3229-9.  p. 72.
  80. ^ a b Creighton, Sarah; Alderson, J; Brown, S; Minto, Cathy (2002). "Medical photography: ethics, consent and the intersex patient". BJU international. 89: 67–71. doi:10.1046/j.1464-410X.2002.02558.x.  p. 70.
  81. ^ "How common is intersex? | Intersex Society of North America". Isna.org. Retrieved 21 August 2009. 
  82. ^ Resolution 1952/2013, Provision version, Children’s right to physical integrity, Council of Europe, 1 October 2013
  83. ^ World Health Organization; OHCHR; UN Women; UNAIDS; UNDP; UNFPA; UNICEF (2014). Eliminating forced, coercive and otherwise involuntary sterilization, An interagency statement (PDF). ISBN 978 92 4 150732 5. 
  84. ^ United Nations High Commissioner for Human Rights (May 4, 2015), Discrimination and violence against individuals based on their sexual orientation and gender identity 
  85. ^ Star Observer (2 April 2015). "Malta passes law outlawing forced surgical intervention on intersex minors". Star Observer. 

References[edit]