Sugarman syndrome

Sugarman syndrome
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. Retrieved 2007-04-02.
  2. ^ Office of Rare Diseases (July 19, 2006). "Sugarman Syndrome". National Institutes of Health. Retrieved 2007-04-02.

 

Prefix: a b c d e f g h i j k l m n o p q r s t u v w x y z 0 1 2 3 4 5 6 7 8 9

Portal di Ensiklopedia Dunia