Rapp–Hodgkin syndrome

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]

See also

• Punctate porokeratosis
• List of cutaneous conditions