Rapp–Hodgkin syndrome

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Rapp–Hodgkin syndrome
Classification and external resources
OMIM 129400

Rapp–Hodgkin syndrome was formerly thought to be a unique autosomal dominant disorder due to a P63 gene mutation. However, it was recently shown to the same disease as Hay-Wells syndrome. [1]

It was first characterized in 1968.[2]

See also[edit]

References[edit]

  1. ^ Clements SE, Techanukul T, Holden ST et al. (September 2010). "Rapp-Hodgkin and Hay-Wells ectodermal dysplasia syndromes represent a variable spectrum of the same genetic disorder". Br. J. Dermatol. 163 (3): 624–9. doi:10.1111/j.1365-2133.2010.09859.x. PMID 20491771. 
  2. ^ Rapp RS, Hodgkin WE (December 1968). "Anhidrotic ectodermal dysplasia: autosomal dominant inheritance with palate and lip anomalies". J. Med. Genet. 5 (4): 269–72. doi:10.1136/jmg.5.4.269. PMC 1468665. PMID 5713637. 

External links[edit]