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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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| Gepubliceerd in: | Front Neurol |
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| Hoofdauteurs: | , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Frontiers Media S.A.
2021
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| Onderwerpen: | |
| Online toegang: | 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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