Results 11 to 20 of about 595 (159)

Diagnostic and Management Strategies of Bietti Crystalline Dystrophy: Current Perspectives [PDF]

open access: yesClinical Ophthalmology, 2023
Ali Osman Saatci,1 Ferdane Ataş,2 Gökhan Ozan Çetin,3 Mustafa Kayabaşı1 1Department of Ophthalmology, Dokuz Eylul University, Izmir, Turkey; 2Department of Ophthalmology, Çerkezköy State Hospital, Tekirdağ, Turkey; 3Department
Saatci AO   +3 more
doaj   +6 more sources

Expanding the Phenotypic and Genotypic Spectrum of Bietti Crystalline Dystrophy [PDF]

open access: yesGenes, 2021
The rare form of retinal dystrophy, Bietti crystalline dystrophy, is associated with variations in CYP4V2, a member of the cytochrome P450 family. This study reports patients affected by typical and atypical Bietti crystalline dystrophy, expanding the spectrum of this disease.
Mariana Matioli Da Palma   +2 more
exaly   +8 more sources

Outcome of macular hole surgery in Bietti crystalline dystrophy [PDF]

open access: yesJournal of Ophthalmic & Vision Research, 2017
Purpose: To describe a 42-year-old man, a known case of Bietti crystalline dystrophy who underwent surgery for unilateral full thickness macular hole.
Ramin Nourinia   +2 more
doaj   +5 more sources

Multimodal Imaging Observation in Different Progressive Types of Bietti Crystalline Dystrophy [PDF]

open access: yesJournal of Ophthalmology, 2022
Objective. The aim of the study is to observe the difference in progression between type 1 and type 2 Bietti crystalline dystrophy (BCD) using multimodal imaging. Methods.
Shengjuan Zhang   +8 more
doaj   +4 more sources

Quickly diagnosing Bietti crystalline dystrophy with deep learning [PDF]

open access: yesiScience
Summary: Bietti crystalline dystrophy (BCD) is an autosomal recessive inherited retinal disease (IRD) and its early precise diagnosis is much challenging.
Haihan Zhang   +7 more
doaj   +5 more sources

Bietti crystalline dystrophy complicated by choroidal neovascularization treated with a single dose of aflibercept

open access: yesOman Journal of Ophthalmology, 2023
Bietti crystalline dystrophy is a rare hereditary autosomal recessive disease that causes photoreceptor loss secondary to degeneration of retinal pigment epithelium due to intracellular retinal pigment epithelial crystalline deposits and abnormal lipid ...
Merve Ozbek   +2 more
doaj   +3 more sources

Unilateral macular neovascularization formation during the follow-up of a 15-year-old boy with Bietti crystalline dystrophy and the successful treatment outcome with a single intravitreal ranibizumab injection [PDF]

open access: yesGMS Ophthalmology Cases, 2023
Objective: To report the successful outcome with a single intravitreal ranibizumab injection in a 15-year-old boy with Bietti crystalline dystrophy (BCD) who developed a unilateral macular neovascularization (MNV)Methods: A retrospective case ...
Kayabaşi, Mustafa   +2 more
doaj   +3 more sources

Longitudinal quantitative assessment of retinal crystalline deposits in bietti crystalline dystrophy [PDF]

open access: yesBMC Ophthalmology
Background This study aims to quantitatively analyze retinal crystalline deposits in patients with Bietti Crystalline Dystrophy (BCD) and examine their progression over time in a longitudinal study.
Seung Jun You   +4 more
doaj   +3 more sources

Foveolar thickness as potential standardized structural outcome measurement in studies of Bietti crystalline dystrophy [PDF]

open access: yesScientific Reports, 2022
Bietti crystalline dystrophy (BCD) is an ultra-rare orphan disorder that can lead to blindness. Because of the variable rates of progression of the disease, it is necessary to identify suitable outcome measurements for tracking progression in BCD.
Laura A. Jenny   +7 more
doaj   +3 more sources

Asymptomatic Unilateral Full-Thickness Macular Hole in a Patient with Bietti Crystalline Dystrophy During 13-Year Follow-up with Optical Coherence Tomography [PDF]

open access: yesTürk Oftalmoloji Dergisi, 2022
A 39-year-old woman with progressive bilateral visual decline was diagnosed as having Bietti crystalline dystrophy in 2008. The disease course was monitored with optical coherence tomography until 2021.
Ali Osman Saatci   +2 more
doaj   +3 more sources

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