Clinical Presentation of Usher Syndrome Type 1B (USH1B) in a 10-Month-Old: A Case Report

Usher Syndrome (USH) is a genetically inherited condition characterized by congenital sensorineural hearing loss and progressive vision loss secondary to retinitis pigmentosa. Patients may also display vestibular areflexia and balance issues secondary to inner ear damage. Usher Syndrome is the most...

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Detalles Bibliográficos
Autores principales: Filson, Meghan J, Davis, Dakota C, Yother, Claire
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Ophthalmology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10513348/
https://www.ncbi.nlm.nih.gov/pubmed/37746462
http://dx.doi.org/10.7759/cureus.43934

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10513348/
https://www.ncbi.nlm.nih.gov/pubmed/37746462
http://dx.doi.org/10.7759/cureus.43934

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