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Medical condition From Wikipedia, the free encyclopedia
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]
Rapp–Hodgkin syndrome | |
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This condition is inherited in an autosomal dominant manner. | |
Specialty | Medical genetics |
It was first characterized in 1968.[2]
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