Sugarman syndrome
From Wikipedia, the free encyclopedia
Sugarman syndrome Classification and external resources |
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OMIM | 258850 | |
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DiseasesDB | 31980 | |
MeSH | C05.116.099.370.652 |
Sugarman syndrome is the common name of autosomal recessive oral-facial-digital syndrome type III, one of ten distinct genetic disorders that involve developmental defects to the mouth.[1]
Alternative names for this condition include: Brachydactyly of the hands and feet with duplication of the first toes, Sugarman brachydactyly and Brachydactyly with major proximal phalangeal shortening.[2]
[edit] References
- ^ Oral-Facial-Digital Syndrome. National Organization for Rare Disorders (2006). Retrieved on 2007-04-02.
- ^ Office of Rare Diseases (July 19, 2006). Sugerman Syndrome. National Institutes of Health. Retrieved on 2007-04-02.