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Anatomic Malformations of the Middle and Inner Ear in 22q11.2 Deletion Syndrome: Case Series and Literature Review

BACKGROUND AND PURPOSE: The 22q11.2 deletion syndrome is characterized by a heterogenic phenotype, including hearing loss. The underlying cause of hearing loss, especially sensorineural hearing loss, is not yet clear. Therefore, our objective was to describe anatomic malformations in the middle and...

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Detalhes bibliográficos
Publicado no:AJNR Am J Neuroradiol
Main Authors: Verheij, E., Elden, L., Crowley, T.B., Pameijer, F.A., Zackai, E.H., McDonald-McGinn, D.M., Thomeer, H.G.X.M.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Neuroradiology 2018
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7410659/
https://ncbi.nlm.nih.gov/pubmed/29545254
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3174/ajnr.A5588
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