Rett syndrome

Rett syndrome
Specialty	Pediatrics, psychiatry, neurology

Rett syndrome (Rett syndrome, Rett's disorder) is a progressive neurological disorder. The symptoms of this disorder are easily confused with those of autism and cerebral palsy. It is recesive inherited and can be carried in a week form for generations dormant with symptoms of learning disorder and total disability to socialize. The clinical diagnosis includes small head, hands, and feet. Stereotypical repetitive hand movements such as mouthing or wringing are also included. Girls are very prone to seizures, GI disorders, and are typically nonverbal. About 50% of the girls/women are ambulatory.

Etiology

Rett syndrome (symbolized RTT) is X-linked dominant, affecting almost exclusively girls. Development is normal until 1 year of age, when language and motor milestones regress and acquired microcephaly is seen. Hand wringing and sighing are characteristic, and they develop autistic behavior. Rett syndrome is usually caused by a mutation in the gene encoding methyl-CpG-binding protein-2 (MECP2). MECP2 is found on chromosome band Xq28, near the long end of the X chromosome. Rett syndrome can also be caused by a mutation to the gene encoding cyclin-dependent kinase-like 5 (CDKL5). Rett syndrome affects 1 in every 12,500 female live births.

Gender and Rett syndrome

Most individuals with Rett syndrome are female. One explanation given for this was that the genetic defect that caused Rett syndrome in females caused embryonic lethality in males (that is, males with pathogenic MECP2 mutations died before they were born). While a plausible hypothesis, more recent research has contradicted this explanation.

Most males with a pathogenic MECP2 mutation suffer from neonatal encephalopathy and die within a year or so of birth. Males who have two X chromosomes and a Y chromosome (often called Klinefelter's syndrome), one with a mutated MECP2 gene, follow a similar development path to females with Rett syndrome. Males who have somatic mosaicism also have symptoms like females with Rett syndrome.

Some researchers (for example Masuyama et al 2005) have reported cases of males with Rett syndrome who have a pathogenic MECP2 mutation but do not have a somatic mosaicism or an extra chromosome.

Unlike most genetic diseases, many cases of Rett syndrome involve spontaneous mutations in one of the parent’s gonads. It has been argued that one cause of the majority of Rett syndrome individuals being female is that mutations to MECP2 are possibly more common in male gonads than female gonads, and only females can inherit a mutated MECP2 gene from fathers (males inherit a Y chromosome from fathers, which does not contain a copy of MECP2).

Development and Symptoms

Infants typically develop normally up to age 6-18 months. Physioneurological development tends to plateau after this brief period of normal development, and is followed by deterioration of high brain functions. Psychomotor and cognitive abilities rapidly decline within 1-2 years of age. Symptoms that develop are autistic-like, with mental retardation and poor growth. It is, hence, easy for the misdiagnosis of Rett for autism, or cerebral palsy.

Autistic-like symptoms in Rett disorder:

• screaming fits
• panic-like attacks
• inconsolable crying
• avoids looking into other people's eyes
• lack of social/emotional reciprocity
• general lack of interest
• marked impairment of use of nonverbal behaviors to regulate social interaction
• delay of linguistic development
  • loss of speech

Symptoms in Rett that are also present in cerebral palsy:

• short stature
• severe dementia
• mild learning disability
• hypotonia
• Delayed or absent ability to walk
• gait/movement difficulties
• ataxia
• microencephalopathy - abnormally small head, lack of head growth
• some forms of spasticity
  • wringing of hands
  • Chorea - spasmodic movements of hand or facial muscles
  • dystonia
  • bruxism - grinding of teeth

Symptoms may stabilize for up to a few decades before complications set in, such as:

• epilepsy/seizure
• spastic paraparesis - spasticity or paralysis of the lower limbs

Treatment & Prognosis

Depending of severity of psychomotor, cognitive impairment, 2-15% of patients may achieve a nonretarded level of cognitive and adaptive functioning through various rehabilitation methods. Marriage, success in achieving employment, independent residence can be achieved during adulthood. There is no current cure for Rett disorder.

Treatment of Rett disorder briefly includes:

• increasing communication skills
• counseling
• modifying social difficulties
• behavioral interventions

Treatment usually requires consultantions from:

• speech and language therapist
• psychologist/counselor
• neurologist/neuropsychiatrist

Common prescriptions:

• antidepressants
  • SSRIs
• antipsychotics
• beta-blockers
• opioid antagonists

Common assistive technology:

• wheelchair
• standing frame

Mortality

Males with pathogenic MECP2 mutations usually die during infancy stage from severe encephalopathy, unless they have an extra X chromosome (often described as Klinefelter's syndrome), or have somatic mosaicism.

Females can live up to 40 years or more. Abnormal lab data values on Rett disorder may show:

• EEG abnormalities from 2 years of age
• atypical glycolipids
• elevated levels of beta-endorphins and glutamate
• reduction of substance P
• decreased levels of nerve growth factors

Mortality rate among children with Rett disorder is approximately at 1.2% per year.

High proportion of deaths are abrupt; due to:

• heart conduction problem - abnormally prolonged QT interval on ECG
• spontaneous brainstem dysfunction
• respiratory arrest

External links

• eMedicine.com
• MedicineNet.com
• NIH
• The International Rett Syndrome Association
• RSRF Rett Syndrome Research Foundation
• NCBI OMIM entry