Albinism–deafness syndrome
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| Albinism–deafness syndrome | |
|---|---|
| Classification and external resources | |
| Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
| OMIM | 300700 |
| Patient UK | Albinism–deafness syndrome |
Albinism–deafness syndrome (also known as "Woolf syndrome," and "Ziprkowski–Margolis syndrome") is a condition characterized by congenital neural deafness and a severe or extreme piebald-like phenotype with extensive areas of hypopigmentation.[1]
A locus at Xq26.3-q27.I has been suggested.[2]
It has been suggested that it is a form of Waardenburg syndrome type II.[3]
See also
References
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