Sugarman syndrome
From Wikipedia, the free encyclopedia
OMIM | 258850 | |
---|---|---|
DiseasesDB | 31980 | |
MeSH | C05.116.099.370.652 |
Sugarman syndrome is the common name of Oral-facial-digital syndrome type III one of ten distinct genetic diorders that all 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] Footnotes
- ^ Oral-Facial-Digital Syndrome. National Organization for Rare Disorders (2006). Retrieved on April 2, 2007.
- ^ Office of Rare Diseases (July 19, 2006). Sugerman Syndrome. National Institutes of Health. Retrieved on April 2, 2007.