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Autosomal dominant foveal hypoplasia without visible macular abnormalities and PAX6 mutations.
Matsushita I, Morita H, Kondo H. Matsushita I, et al. Jpn J Ophthalmol. 2020 Nov;64(6):635-641. doi: 10.1007/s10384-020-00766-9. Epub 2020 Aug 28. Jpn J Ophthalmol. 2020. PMID: 32857266 Review.
PURPOSE: Autosomal dominant foveal hypoplasia (FVH1) is a rare disorder associated with mutations in the PAX6 gene. As an isolated disease entity, FVH1 does not include ocular disorders such as aniridia, microphthalmia, albinism, and achromatopsia. However, it only …
PURPOSE: Autosomal dominant foveal hypoplasia (FVH1) is a rare disorder associated with mutations in the PAX6 gene. As an isolated di …
Non-typical persistent hyperplastic primary vitreous: a rare case report and review of the literature.
Yu Y, Qiao Y, Chen S, Hu J, Li J, Yao K, Yu Y. Yu Y, et al. BMC Ophthalmol. 2023 Jun 13;23(1):267. doi: 10.1186/s12886-023-03024-x. BMC Ophthalmol. 2023. PMID: 37312173 Free PMC article. Review.
CASE PRESENTATION: A 68-year-old healthy male was referred to our outpatient department for evaluation of age-related cataract without other visual symptoms. Preoperative fundus examination occasionally detected an isolated stalk-like band extending to the posterior …
CASE PRESENTATION: A 68-year-old healthy male was referred to our outpatient department for evaluation of age-related cataract withou …