A rare case of fundus albipunctatus with a novel RDH5 gene mutation
Fundus albipunctatus (FA) is a rare, genetic retinal dystrophy that belongs to a heterogeneous group of genetically determined flecked retina syndromes. The presence of multiple retinal yellowish-white lesions of various sizes and configurations, without vascular or optic nerve abnormalities are cha...
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| Auteurs principaux: | , , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Wolters Kluwer Medknow Publications
2023-07-01
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| Collection: | Indian Journal of Ophthalmology. Case Reports |
| Sujets: | |
| Accès en ligne: | https://journals.lww.com/10.4103/IJO.IJO_3356_22 |
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