Albinism–deafness syndrome
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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Contributors: Prab R. Tumpati, MD
