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A Very Rare Association of Fuchs Heterochromic Uveitis and Ectropion Uvea in Usher Syndrome
Usher syndrome is a heterogeneous genetic disease that is the most common cause of hereditary blindness–deafness. This syndrome is the most prevalent syndrome associated with retinitis pigmentosa. A 25-year-old man referred to us with hearing loss and vision diminution since childhood which has grad...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Wolters Kluwer - Medknow
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8781905/ https://www.ncbi.nlm.nih.gov/pubmed/35127577 http://dx.doi.org/10.4103/abr.abr_286_20 |