Bilateral cochlear implantation in a child with Waardenburg syndrome: A case report

BackgroundWaardenburg syndrome (WS) is a rare genetic disorder that presents with clinical characteristics such as white forelock, congenital deafness, dystopia canthorum, and heterochromia iridis. It is mostly transmitted through an autosomal dominant mode, with a few genetic mutations. Children wi...

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Príomhchruthaitheoirí: Xiaohui Wang (Údar), Lin Xu (Údar), Na Zhang (Údar), Ying Zhao (Údar)
Formáid: LEABHAR
Foilsithe / Cruthaithe: Frontiers Media S.A., 2022-09-01T00:00:00Z.
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