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Albinism–deafness syndrome
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| Albinism–deafness syndrome | |
|---|---|
| Other names | Woolf syndrome and Ziprkowski–Margolis syndrome |
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| 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]
See also
References
External links
| Classification | |
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