Sugarman syndrome
| Sugarman syndrome | |
|---|---|
| Classification and external resources | |
| OMIM | 258850 |
| 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]
Sugarman syndrome has an autosomal recessive pattern of inheritance.
References
- ↑ "Oral-Facial-Digital Syndrome". National Organization for Rare Disorders. 2006. Retrieved 2007-04-02.
- ↑ Office of Rare Diseases (July 19, 2006). "Sugarman Syndrome". National Institutes of Health. Retrieved 2007-04-02.
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