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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2022-09-01T00:00:00Z.
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