Cochlear Implantation via the Transmeatal Approach in an Adolescent with Hunter Syndrome—Type II Mucopolysaccharidosis

Type II mucopolysaccharidosis (MPS II) commonly known as Hunter syndrome, is a rare X-linked lysosomal storage disorder caused by iduronate-2-sulfatase deficiency, which in turn causes otorhinolaryngological manifestations, including sensorineural hearing loss (SNHL). Previously, the median survival...

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Detalles Bibliográficos
Autores principales: Kim, Hantai, An, Jun Young, Choo, Oak-Sung, Jang, Jeong Hun, Park, Hun Yi, Choung, Yun-Hoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Audiological Society and Korean Otological Society 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7835431/
https://www.ncbi.nlm.nih.gov/pubmed/31813213
http://dx.doi.org/10.7874/jao.2019.00325

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7835431/
https://www.ncbi.nlm.nih.gov/pubmed/31813213
http://dx.doi.org/10.7874/jao.2019.00325

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