Anatomic Malformations of the Middle and Inner Ear in 22q11.2 Deletion Syndrome: Case Series and Literature Review.
- E Verheij,
- L Elden,
- T B Crowley,
- F A Pameijer,
- E H Zackai,
- D M McDonald-McGinn,
- H G X M Thomeer
AJNR Am J Neuroradiol 2018 Mar 15. Epub 2018 Mar 15.
From the Department of Otorhinolaryngology-Head and Neck Surgery (E.V., H.G.X.M.T.).
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. Read More