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Tietz syndrome

MONDO:0007077

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.

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Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Eye disorder (97) Human disease (14) Skin pigmentation disorder (11) Hereditary skin disorder (5) Disorder of orbital region (3) Disease of genetic or genomic mechanism (2) Hypopigmentation of the skin (2)

Trials to join now! 12 Not yet recruiting 1 Not yet finished but already full! 2 Completed 1 Terminated 1

VR headsets tested as a possible treatment for blindness

Disease control Terminated

This study tested whether using a virtual reality headset for one-hour sessions could help regenerate damaged optic nerves and improve vision in people with glaucoma or other retinal diseases. The idea came from promising results in rodents. However, the trial was terminated earl…

Phase: NA • Sponsor: Stanford University • Aim: Disease control

Last updated Jun 27, 2026 08:03 UTC