Rapp–Hodgkin syndrome
From Infogalactic: the planetary knowledge core
| Rapp–Hodgkin syndrome | |
|---|---|
| Classification and external resources | |
| Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
| OMIM | 129400 |
| Patient UK | 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]
It was first characterized in 1968.[2]
See also
References
External links
- GeneReviews/NCBI/NIH/UW entry on Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate Syndrome or AEC Syndrome, Hay-Wells Syndrome. Includes: Rapp-Hodgkin Syndrome
- OMIM entries on AEC
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