Open AccessCase report: Congenital profound deafness and Cochlea Implantation in Tietz syndrome (hypopigmentation/deafness)
Author(s) -
Katie O’Brien,
Katharina Bahr,
Ellen S. Martin,
Dimitrios Koutsimpelas
Publication year - 2018
Publication title -
laryngo-, rhino-, otologie
Language(s) - English
Resource type - Conference proceedings
eISSN - 1438-8685
pISSN - 0935-8943
DOI - 10.1055/s-0038-1640725
Subject(s) - waardenburg syndrome , hypopigmentation , microphthalmia associated transcription factor , cochlea , hearing loss , audiology , medicine , genetics , gene , dermatology , biology , phenotype , transcription factor