Tietz syndrome
From Wikipedia, the free encyclopedia
| OMIM | 103500 |
|---|---|
| DiseasesDB | 34108 |
Tietz syndrome is due to a mutation in chromosome 3, and is characterized by deafness and albinism.
Tietz syndrome is not to be confused with Tietze's syndrome, which is a benign inflammation of the ligaments connecting to the sternum or ribs.
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