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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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| Publicado en: | Front Neurol |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Frontiers Media S.A.
2021
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| Assuntos: | |
| Acceso en liña: | 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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