|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.
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