Sugarman syndrome
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| Sugarman syndrome | |
|---|---|
| Classification and external resources | |
| Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
| OMIM | 258850 |
| DiseasesDB | 31980 |
| Patient UK | Sugarman syndrome |
| 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
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