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Tietz syndrome

rare

Tietz syndrome is a genetic hypopigmentation and deafness syndrome characterized by congenital profound bilateral sensorineural hearing loss and generalized albino-like hypopigmentation of skin, eyes and hair.

Identifiers
MONDO:0007077 OMIM:103500Orphanet:42665
Causal genes
MITF
Part of
Eye disorderHereditary skin disorderHypopigmentation of the skin
Also known as
albinism-deafness of Tietz · hypopigmentation-deafness syndrome · hypopigmentation/deafness of Tietz · TADS · Tietz albinism-deafness syndrome

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