51 top medical experts on Tietz syndrome across 6 countries and 3 U.S. states, including 4 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. 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.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations
  4. Synonyms: Albinism and complete nerve deafness,  Albinism-deafness of Tietz,  Hypopigmentation-deafness of Tietz,  Tietz albinism-deafness syndrome


  

        

                    


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