Cochlear Implantation Outcome in Children with DFNB1 locus Pathogenic Variants

Almost 60% of children with profound prelingual hearing loss (HL) have a genetic determinant of deafness, most frequently two DFNB1 locus (GJB2/GJB6 genes) recessive pathogenic variants. Only few studies combine HL etiology with cochlear implantation (CI) outcome. Patients with profound prelingual H...

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Detalles Bibliográficos
Autores principales: Oziębło, Dominika, Obrycka, Anita, Lorens, Artur, Skarżyński, Henryk, Ołdak, Monika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7019930/
https://www.ncbi.nlm.nih.gov/pubmed/31952308
http://dx.doi.org/10.3390/jcm9010228

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7019930/
https://www.ncbi.nlm.nih.gov/pubmed/31952308
http://dx.doi.org/10.3390/jcm9010228

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