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A 5-year-old Syrian female was born with Oguchi disease: a rare case report
Oguchi disease is a rare autosomal recessive disease that causes congenital stationary blindness, which is distinguished by the Mizuo–Nakamura phenomenon and caused by mutations of rhodopsin kinase gene or the arrestin gene. CASE PRESENTATION: A 5-year-old Syrian female complains of stationary night...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Lippincott Williams & Wilkins
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10129271/ https://www.ncbi.nlm.nih.gov/pubmed/37113844 http://dx.doi.org/10.1097/MS9.0000000000000100 |