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Albinism–deafness syndrome

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Albinism–deafness syndrome
Other namesWoolf syndrome and Ziprkowski–Margolis syndrome
X-linked recessive.svg
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.[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]

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Classification
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