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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. 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.

[ "Genetics", "Gene", "Neuroscience" ]
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