Tietz syndrome

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.

Also known as: Tietz albinism-deafness syndrome, Tietz syndrome, albinism-deafness of Tietz, hypopigmentation-deafness syndrome, hypopigmentation/deafness of Tietz, TADS

17 clinical trials for this condition and its sub-types.