Albinism–deafness syndrome
| Albinism–deafness syndrome | |
|---|---|
| Other names | Woolf syndrome and Ziprkowski–Margolis syndrome |
 | |
| Albinism–deafness syndrome is inherited in an X-linked recessive manner | |
Albinism–deafness syndrome is a condition characterized by congenital neural deafness and a severe or extreme piebald-like phenotype with extensive areas of hypopigmentation.
A locus at Xq26.3-q27.I has been suggested.
It has been suggested that it is a form of Waardenburg syndrome type II.