Alteraciones audiovestibulares de lenguaje y foniátricas en microdeleción 22q11.2.

BACKGROUND: 22q11.2 deletion syndrome is a genetic disorder caused by a hemizygous microdeletion of the long arm of chromosome 22; its worldwide prevalence is 1 in every 2000 to 4000 live births. According to the literature, these patients may present, among other alterations: cardiac malformations,...

Full description

Bibliographic Details

Published in:	Anales de Otorrinolaringología Mexicana Vol. 70; no. 2; pp. 108 - 119
Main Authors:	Barradas Hernández, María Isabel, Lino González, Ana Luisa
Format:	Article
Published:	Sociedad Mexicana de Otorrinolaringologia y Cirugia de Cabeza y Cuello abr-jun2025
Subjects:	Digeorge syndrome Conductive hearing loss Genetic disorders Hearing disorders Learning disabilities
Online Access:	View this record in EBSCOhost