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

1 clinical trial for this condition and its sub-types, 1 tagged with Tietz syndrome itself.

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Where it sits in the disease tree

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Part of

↑ Eye disorder (3068) ↑ Hereditary skin disorder (880) ↑ Hypopigmentation of the skin (21)

Including sub-types (1) Tagged with Tietz syndrome (1)

Not yet finished but already full! 1

Which Mini-Implant size works best? new study aims to find out

Knowledge-focused Ongoing

This study tests two different diameters (1.6mm and 2mm) of mini-implants placed in the upper jaw to support orthodontic tooth movement. Twenty people receiving braces will get one size on each side of their mouth. Researchers will measure how stable the implants are, how much pa…

Sponsor: University of Baghdad • Aim: Knowledge-focused

Last updated Sep 18, 2026 00:00 UTC

Tietz syndrome

Where it sits in the disease tree

Which Mini-Implant size works best? new study aims to find out