Tietz syndrome

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Tietz syndrome Classification and external resources
OMIM	103500
DiseasesDB	34108

Tietz syndrome is a condition characterized by deafness and albinism.

It is due to a mutation in chromosome 3, possibly in the microphthalmia-associated transcription factor.

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.

Acknowledgement and Attribution Regarding Sources of Content

Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .