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

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
Main Authors: Kwang-Dong Choi, Jeong-Yeon Kim, Seo-Young Choi, Eun Hye Oh, Hyun-Min Lee, Jieun Roh, Jae-Hwan Choi
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-06-01
Series:Frontiers in Neurology
Subjects:
22q112 deletion syndrome
Ménière's disease
endolymphatic hydrops
case report
vertigo
sensorineural hearing loss
Online Access:https://www.frontiersin.org/articles/10.3389/fneur.2021.690078/full

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https://www.frontiersin.org/articles/10.3389/fneur.2021.690078/full

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