Rapp–Hodgkin syndrome
Rapp–Hodgkin syndrome | |
---|---|
Other names | Ectodermal dysplasia, anhidrotic, with cleft lip/palate[1] |
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.[2]
It was first characterized in 1968.[3]
See also
- Punctate porokeratosis
- List of cutaneous conditions
References
- ^ "Rapp–Hodgkin syndrome". The Genetic and Rare Diseases Information Center. NIH. Retrieved 19 March 2019.
- S2CID 44866051.
- PMID 5713637.
Further reading
External links