Sugarman syndrome
| Sugarman syndrome | ||
| 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 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]
Footnotes
- ↑ "Oral-Facial-Digital Syndrome". National Organization for Rare Disorders. 2006. Retrieved 2007-04-02.
- ↑ Office of Rare Diseases (July 19, 2006). "Sugerman Syndrome". National Institutes of Health. Retrieved 2007-04-02.