Hirschsprung's disease-type D brachydactyly syndrome
| Hirschsprung's disease-brachydactyly type D syndrome | |
|---|---|
| Other names | Familial Hirschsprung's disease and brachydactyly type D |
| Specialty | Medical genetics |
| Symptoms | hirschsprung's disease and brachydactyly type D |
| Causes | Genetic mutation |
| Prevention | none |
| Frequency | Hirschsprung's disease: 1 in 5,000 live births.,[1] brachydactyly type D: 3% of the world population |
Hirschsprung's disease-type D brachydactyly syndrome is a very rare genetic disorder which is characterized by the partial absence of nerves in the intestines (Hirschsprung's disease) and hypoplasia (or total aplasia) of the thumb's distal phalange (brachydactyly type D).[2][3] It has been described in 4 males from a 2-generation American family. The inheritance pattern was hypothesized to be either X-linked recessive or autosomal dominant with reduced penetrance.[4][5]
References
[edit]- ^ "Hirschsprung disease: MedlinePlus Genetics".
- ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Hirschsprung disease type D brachydactyly syndrome". www.orpha.net. Retrieved 2022-05-15.
{{cite web}}: CS1 maint: numeric names: authors list (link) - ^ "Hirschsprung disease type d brachydactyly - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Retrieved 2022-05-15.
- ^ "OMIM Entry - 306980 - HIRSCHSPRUNG DISEASE WITH TYPE D BRACHYDACTYLY". omim.org. Retrieved 2022-05-15.
- ^ Reynolds, J. F.; Barber, J. C.; Alford, B. A.; Chandler, J. G.; Kelly, T. E. (February 1983). "Familial Hirschsprung's disease and type D brachydactyly: a report of four affected males in two generations". Pediatrics. 71 (2): 246–249. doi:10.1542/peds.71.2.246. ISSN 0031-4005. PMID 6823428. S2CID 45422912.
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