Caudal regression syndrome

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Caudal regression syndrome
Other names: Sacral regression sequence, Sacral agenesis
Sacral agenesis

Caudal regression syndrome, or sacral agenesis (or hypoplasia of the sacrum), is a rare birth defect. It is a congenital disorder in which the fetal development of the lower spine—the caudal partition of the spine—is abnormal.[1] It occurs at a rate of approximately one per 60,000 live births.[2]

Some babies are born with very small differences compared to typical development, and others have significant changes. Most grow up to be otherwise typical adults who have difficulty with walking and incontinence.

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.[citation needed]

Cause

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 has a combination of environmental and genetic causes, and that various types of the condition may have differing causes.[citation needed]

Sacral agenesis syndrome (a type of caudal regression syndrome involving 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.[3][4] Other causes are presumably involved, as demonstrated by the rare overall incidence of caudal regression syndrome (1:60,000) compared to diabetes; however, the condition does have a greatly increased incidence among infants born to mothers with diabetes, estimated at 1 in 350 newborns of mothers with diabetes.[2]

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).[citation needed]

It was previously thought to be related to sirenomelia ("Mermaid syndrome") but has now been determined not to be related to this condition.[5]

Diagnosis

  • Caudal regression syndrome-a) Brain MRI shows 2 cystic structures at the region of cisterna magna b) cyst is also shown on axial T2-weighted image c) MRI dorsolumbar spine showing abrupt cutoff and bulbar configuration of conus medullaris at the level of L1

    Caudal regression syndrome-a) Brain MRI shows 2 cystic structures at the region of cisterna magna b) cyst is also shown on axial T2-weighted image c) MRI dorsolumbar spine showing abrupt cutoff and bulbar configuration of conus medullaris at the level of L1

  • Antero-posterior radiographic view, showing missing ribs, absent lumbosacral vertebrae, hypoplastic pelvis and "frog-like" position of the lower extremities

    Antero-posterior radiographic view, showing missing ribs, absent lumbosacral vertebrae, hypoplastic pelvis and "frog-like" position of the lower extremities

In terms of the diagnosis of Caudal regression syndrome we find that the following is used:[6]

Management

Treatment is symptom specific; there may be a need for surgery(ies) and/or anticholinergic drugs as the clinical situation dictates.[6]

Prognosis

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.[citation needed]

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. The condition often impacts the formation of the knees, legs or feet that is sometimes addressed through surgery. For some with tightly webbed, bent knees or knees that are fused straight, disarticulation surgery at the knee may be a viable option to maximize mobility options.[citation needed]

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 increase. 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.[citation needed]

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 Mount Kilimanjaro using only his hands.[7] In 2021, athlete Zion Clark broke the Guinness World Record 20m running on hands.[8]

Society and culture

Notable people

References

  1. ↑ 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.
  2. ↑ 2.0 2.1 Medline Plus. Caudal Regression Syndrome.https://medlineplus.gov/genetics/condition/caudal-regression-syndrome/#frequency Archived 2022-05-20 at the Wayback Machine
  3. ↑ Al Kaissi, Ali; Klaushofer, Klaus; Grill, Franz (19 December 2008). "Caudal regression syndrome and popliteal webbing in connection with maternal diabetes mellitus: a case report and literature review". Cases Journal. 1 (1): 407. doi:10.1186/1757-1626-1-407. PMC 2614953. PMID 19099562.
  4. ↑ Zaw, Win; Stone, David G. (March 2002). "Caudal Regression Syndrome in Twin Pregnancy With Type II Diabetes". Journal of Perinatology. 22 (2): 171–174. doi:10.1038/sj.jp.7210614. PMID 11896527. S2CID 10374738.
  5. ↑ "Sirenomelia". Archived from the original on 2022-01-14. Retrieved 2022-05-03.
  6. ↑ 6.0 6.1 "Caudal Regression Syndrome". NORD (National Organization for Rare Disorders). Archived from the original on 11 October 2021. Retrieved 21 June 2022.
  7. ↑ "Man Climbs Mt. Kilimanjaro On Hands". ABC News. 22 June 2012. Archived from the original on 13 December 2017. Retrieved 3 May 2022.
  8. ↑ "Zion Clark achieves record for fasted 20m on hands". Guinness World Records. 22 September 2021. Archived from the original on 3 April 2022. Retrieved 3 May 2022.
  9. ↑ Karimi, Faith; Sutton, Joe (13 December 2015). "'American Horror Story' actress Rose Siggins dead at 43". CNN. Archived from the original on 23 June 2022. Retrieved 3 May 2022.

External links

Classification
External resources
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