Medicine:Sugarman syndrome

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Sugarman syndrome
Autorecessive.svg
Sugarman syndrome has an autosomal recessive pattern of inheritance.

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]

References

  1. "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. 
  2. Office of Rare Diseases (July 19, 2006). "Sugarman Syndrome". National Institutes of Health. http://rarediseases.info.nih.gov/GARD/Disease.aspx?PageID=4&diseaseID=5058&Expanded=true. Retrieved 2007-04-02. 

External links

Classification
External resources