Vestibular Function in Children With Von Hippel–Lindau Disease

Von Hippel–Lindau disease (VHL) is a rare autosomal dominant disorder. It is caused by a mutation in the tumor suppressor gene localized at 3p25-26. Endolymphatic sac tumors (ELSTs) are rare low-grade adenocarcinomas which can occur sporadically but are more commonly found in association with VHL di...

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Detalles Bibliográficos
Autores principales: Fatih Turgut, Nesrettin, Crunkhorn, Rosa, Iqbal, Javed, Dasgupta, Soumit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Academy of Otology and Neurotology and the Politzer Society 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9450049/
https://www.ncbi.nlm.nih.gov/pubmed/34309559
http://dx.doi.org/10.5152/iao.2021.0190

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9450049/
https://www.ncbi.nlm.nih.gov/pubmed/34309559
http://dx.doi.org/10.5152/iao.2021.0190

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