Rare Gene Mutations in Romanian Hypoacusis Patients: Case Series and a Review of the Literature

(1) Background: In this paper, we report on three cases of hypoacusis as part of a complex phenotype and some rare gene variants. An extensive review of literature completes the newly reported clinical and genetic information. (2) Methods: The cases range from 2- to 11-year-old boys, all with a comp...

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Detalles Bibliográficos
Autores principales: Neagu, Alexandra-Cristina, Budișteanu, Magdalena, Gheorghe, Dan-Cristian, Mocanu, Adela-Ioana, Mocanu, Horia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9501263/
https://www.ncbi.nlm.nih.gov/pubmed/36143929
http://dx.doi.org/10.3390/medicina58091252

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9501263/
https://www.ncbi.nlm.nih.gov/pubmed/36143929
http://dx.doi.org/10.3390/medicina58091252

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