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
Hay–Wells syndrome (also known as AEC syndrome; see ''Naming'') is one of at least 150 known types of ectodermal dysplasia. These disorders affect tissues that arise from the ectodermal germ layer, such as skin, hair, and nails.
Genetics
Ha ...
.
It was first characterized in 1968.
See also
*
Punctate porokeratosis
*
List of cutaneous conditions
References
Further reading
GeneReviews/NCBI/NIH/UW entry on Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate Syndrome or AEC Syndrome, Hay–Wells Syndrome. Includes: Rapp–Hodgkin Syndrome
External links
OMIM entries on AEC
Genodermatoses
Rare syndromes
{{Genodermatoses-stub