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

BACKGROUND: Waardenburg 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...

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Detalles Bibliográficos
Autores principales: Wang, Xiaohui, Xu, Lin, Zhang, Na, Zhao, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9510376/
https://www.ncbi.nlm.nih.gov/pubmed/36172395
http://dx.doi.org/10.3389/fped.2022.965884

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9510376/
https://www.ncbi.nlm.nih.gov/pubmed/36172395
http://dx.doi.org/10.3389/fped.2022.965884

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