Retinal findings in pediatric patients with Usher syndrome Type 1 due to mutations in MYO7A gene

PURPOSE: To describe retinal alterations detected by swept-source optical coherence tomography (SS-OCT) in paediatric patients with Usher syndrome type 1 (USH1) and to compare these findings to previously published reports. METHODS: Thirty-two eyes from 16 patients (11 males and 5 females) with a ge...

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Publicado en:Eye (Lond)
Autores principales: Subirà, Olaia, Català-Mora, Jaume, Díaz-Cascajosa, Jesús, Padrón-Pérez, Noel, Claveria, M. A., Coll-Alsina, Natalia, Bonnet, Crystel, Petit, Christine, Caminal, J. M., Prat, Joan
Formato: Artigo
Lenguaje:Inglês
Publicado: Nature Publishing Group UK 2019
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC7042307/
https://ncbi.nlm.nih.gov/pubmed/31320737
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41433-019-0536-6
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