Sugarman syndrome
Medical condition / From Wikipedia, the free encyclopedia
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]
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Sugarman syndrome | |
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Sugarman syndrome has an autosomal recessive pattern of inheritance. |
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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]