- Sugarman syndrome
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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. http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Oral-Facial-Digital%20Syndrome. Retrieved 2007-04-02.
- ^ Office of Rare Diseases (July 19, 2006). "Sugerman Syndrome". National Institutes of Health. http://rarediseases.info.nih.gov/GARD/Disease.aspx?PageID=4&diseaseID=5058&Expanded=true. Retrieved 2007-04-02.
Categories:- Autosomal recessive disorders
- Rare diseases
- Syndromes
- Disease stubs
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