Clinical Biochemical and Pathologic Correlations in Bietti's Crystalline Dystrophy
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Cited by (111)
Intereye Symmetry in Bietti Crystalline Dystrophy
2022, American Journal of OphthalmologyAnalysis of Radial Peripapillary Capillary Density in Patients with Bietti Crystalline Dystrophy by Optical Coherence Tomography Angiography
2022, Biomedical and Environmental SciencesSyndromic retinal disease
2022, Clinical Ophthalmic Genetics and GenomicsCYP4V2 mutation screening in an Iranian Bietti crystalline dystrophy pedigree and evidence for clustering of CYP4V2 mutations
2019, Journal of Current OphthalmologyOCT angiography and evaluation of the choroid and choroidal vascular disorders
2018, Progress in Retinal and Eye ResearchCitation Excerpt :The main sites of expression of this gene in the eye are the RPE and choroid. In advanced cases, histopathology demonstrates severe panchorioretinal atrophy, with crystals and complex lipid inclusions seen in choroidal fibroblasts, corneal keratocytes, and conjunctival fibroblasts (Kaiser-Kupfer et al., 1994; Wilson et al., 1989). Choroidal involvement is thought to be central to the pathogenesis of this condition.
Corneal deposits and nerve alterations in Bietti Corneoretinal Crystalline Dystrophy imaged using in vivo confocal microscopy
2023, Graefe's Archive for Clinical and Experimental Ophthalmology
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