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Schmitt Gillenwater Kelly syndrome information


Schmitt Gillenwater Kelly syndrome
Other namesRadial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome
Schmitt Gillenwater Kelly syndrome has an autosomal dominant pattern of inheritance.

Schmitt Gillenwater Kelly syndrome is a rare autosomal dominant[1] congenital disorder consisting of radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema.[1][2]

  1. ^ a b Cite error: The named reference sad was invoked but never defined (see the help page).
  2. ^ Cite error: The named reference rar was invoked but never defined (see the help page).

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Schmitt Gillenwater Kelly syndrome

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