Rapp–Hodgkin syndrome
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 | |
|---|---|
| |
| This condition is inherited in an autosomal dominant manner. | |
| Specialty | Medical genetics |
It was first characterized in 1968.[2]