Case Report: Ménière's Disease-Like Symptoms in 22q11.2 Deletion Syndrome

The 22q11.2 deletion syndrome (22q11.2DS), caused by a microdeletion on the long arm of chromosome 22, is characterized by congenital heart disease, hypoparathyroidism, immunodeficiency, developmental delay, and velopharyngeal insufficiency. Anatomic malformations of the middle and inner ears are fr...

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Detalles Bibliográficos
Autores principales: Choi, Kwang-Dong, Kim, Jeong-Yeon, Choi, Seo-Young, Oh, Eun Hye, Lee, Hyun-Min, Roh, Jieun, Choi, Jae-Hwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8250142/
https://www.ncbi.nlm.nih.gov/pubmed/34220691
http://dx.doi.org/10.3389/fneur.2021.690078

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8250142/
https://www.ncbi.nlm.nih.gov/pubmed/34220691
http://dx.doi.org/10.3389/fneur.2021.690078

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