Caudal regression syndrome
|Caudal regression syndrome|
|Synonyms||Sacral regression sequence, Sa|
Caudal regression syndrome, or sacral agenesis (or hypoplasia of the sacrum), is a congenital disorder in which there is abnormal fetal development of the lower spine—the caudal partition of the spine. It occurs at a rate of approximately one per 25,000 live births.
Signs and symptoms
This condition exists in a variety of forms, ranging from partial absence of the tail bone regions of the spine to absence of the lower vertebrae, pelvis and parts of the thoracic and/or lumbar areas of the spine. In some cases where only a small part of the spine is absent, there may be no outward sign of the condition. In cases where more substantial areas of the spine are absent, there may be fused, webbed or smaller lower extremities and paralysis. Bowel and bladder control is usually affected.
The condition arises from some factor or set of factors present during approximately the 3rd week to 7th week of fetal development. Formation of the sacrum/lower back and corresponding nervous system is usually nearing completion by the 4th week of development. Due to abnormal gastrulation, the mesoderm migration is disturbed. This disturbance results in symptoms varying from minor lesions of the lower vertebrae to more severe symptoms such as complete fusion of the lower limbs. While the exact cause is unknown, it has been speculated that the condition may be associated with certain dietary deficiencies including a lack or insufficient amounts of folic acid.
Sacral agenesis syndrome (agenesis of the lumbar spine, sacrum, and coccyx, and hypoplasia of the lower extremities) is a well-established congenital anomaly associated with maternal diabetes mellitus (not gestational diabetes). However, other causes are presumably involved, as demonstrated by the rare incidence of caudal regression syndrome (1:60,000) compared to diabetes.
The dominant inherited sacral agenesis (also referred to as Currarino syndrome) is very often correlated with a mutation in the Hb9 (also called HlxB9) gene (shown by Sally Ann Lynch, 1995, Nature Genetics).
It was previously thought to be related to sirenomelia ("Mermaid syndrome") but has now been determined not to be related to this condition.
There are four levels (or "types") of malformation. The least severe indicates partial deformation (unilateral) of the sacrum. The second level indicates a bilateral (uniform) deformation. The most severe types involve a total absence of the sacrum.
Depending on the type of sacral agenesis, bowel or urinary bladder deficiencies may be present. A permanent colostomy may be necessary in the case of imperforate anus. Incontinence may also require some type of continence control system (e.g., self-catheterization) be utilized. Occasionally if deformities of the knees, legs or feet would prove unresponsive to corrective action, amputation at the knee may be proposed.
Before more comprehensive medical treatment was available, full amputation of the legs at the hip was often performed. More recently, the 'amputation' (actually a disarticulation because no cutting of the bone is involved) is done at the knee for those who have bent knee positions and webbing between thigh and calf to enable more ease of mobility and better seating. Some children with knee disarticulation use prosthetic legs to walk. Prosthetics for children without substantial hip and trunk control is usually abandoned in favor of faster and easier wheelchair mobility as the child's weight and age increases. Children may 'walk' on their hands and generally are able to climb and move about to accomplish whatever they need and want to accomplish. Children more mildly affected may have normal gait and no need for assistive devices for walking. Others may walk with bracing or crutches.
There is typically no cognitive impairment associated with this disability. Adults with this disability live independently, attend college, and have careers in various fields. In 2012, Spencer West, a man with sacral agenesis and both legs amputated, climbed Mt. Kilimanjaro using only his hands.
- Johnny Eck, American freak show performer
- Kenny Easterday, played a fictionalized version of himself in the film Kenny
- Kurt Fearnley, Australian wheelchair racer
- Bobby Martin, American footballer
- Jessica Rogers, American wheelchair racer and swimmer, founder and President of iSACRA (International Caudal Regression Syndrome Association)
- Rose Siggins, actress (American Horror Story: Freak Show)
- Spencer West, Canadian motivational speaker, social activist
- Victoria Pendergast, first female Australian sit-skier at Winter Paralympics
- Kendra (Sanders) Schraml, Ms. Wheelchair Washington 2011
- Piyah Martell, YouTuber and guest star on RuPaul’s Drag Race
- Rebecca Dubber, New Zealand para-swimmer and Rio 2016 Paralympic bronze medalist
- Kevin McKee, two-times olympic champion and two-times world champion in sledge hockey
- Zion Clark, college wrestler at Kent State University at Tuscarawas, star of Netflix documentary, Zion
- Sonek JD, Gabbe SG, Landon MB, Stempel LE, Foley MR, Shubert-Moell K (March 1990). "Antenatal diagnosis of sacral agenesis syndrome in a pregnancy complicated by diabetes mellitus". Am. J. Obstet. Gynecol. 162 (3): 806–8. doi:10.1016/0002-9378(90)91015-5. PMID 2180307.
- News, A. B. C. (22 June 2012). "Man Climbs Mt. Kilimanjaro On Hands". ABC News.
- CNN, Faith Karimi and Joe Sutton,. "'American Horror Story' actress Rose Siggins dead at 43 - CNN". cnn.com.
- "Pageant title helps spread message about disabilities". championnewspapers.com.
- Ellwood, Deb (10 January 2018). "Kent State Tuscarawas Golden Eagles Wrestler Zion Clark Makes No Excuses". Retrieved 12 August 2018.