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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Bibliographic Details
Published in:Front Neurol
Main Authors: Choi, Kwang-Dong, Kim, Jeong-Yeon, Choi, Seo-Young, Oh, Eun Hye, Lee, Hyun-Min, Roh, Jieun, Choi, Jae-Hwan
Format: Artigo
Language:Inglês
Published: Frontiers Media S.A. 2021
Subjects:
Neurology
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC8250142/
https://ncbi.nlm.nih.gov/pubmed/34220691
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2021.690078
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