Subtle Malformation of the Cochlear Apex and Genetic Abnormalities: Beyond the "Thorny" Cochlea.
AJNR Am J Neuroradiol
; 44(1): 79-81, 2023 01.
Article
em En
| MEDLINE
| ID: mdl-36549853
ABSTRACT
With the routine use of high-resolution heavily T2-weighted sequences to evaluate patients with hearing deficits, new, subtle phenotypes of cochlear malformations are being discovered and an increasing number of genotype-phenotype correlations are being found through a reverse phenotype approach, which can help guide geneticists. In this brief report, we present subtle malformations of the apical turn of the cochlea related to 3 genetic mutations, emphasizing the importance of a careful assessment of the cochlear apex.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Cóclea
/
Implante Coclear
Idioma:
En
Ano de publicação:
2023
Tipo de documento:
Article