Case Report: Clinical and genetic analysis of a Bietti crystalline dystrophy family with multisite crystalline deposits and a phenotype of macular hole combined with retinoschisis [PDF]
PurposeTo identify and characterize the genetic mutation responsible for Bietti crystalline dystrophy (BCD) in a Chinese consanguineous family and to describe the associated clinical phenotypes.MethodsComprehensive genetic screening was performed on a ...
Cheng-yao Zheng +3 more
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Role of red free imaging, retinal reflectance and fundus autofluorescence in Bietti crystalline dystrophy: case report [PDF]
Bietti crystalline dystrophy (BCD), a rare autosomal recessive hereditary disorder, is identified by its clinical features. It is characterised by crystalline deposits and hence called crystalline retinopathy. The retinopathy progresses with age, showing
Abhidnya Surve +5 more
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Macular cysts in bietti crystalline dystrophy
Bietti crystalline dystrophy (BCD) is a rare autosomal disorder characterized by the presence of intraretinal crystalline deposits and later chorioretinal degeneration. We describe a case of BCD with macular cysts.
Syed Mohideen Abdul Khadar +2 more
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We report a rare case of Bietti′s crystalline dystrophy presenting with choroidal neovascular membrane (CNVM) which was treated with three injections of intravitreal ranibizumab.
Kasinathan Nachiappan +2 more
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A novel mutation of CYP4V2 gene associated with Bietti crystalline dystrophy complicated by choroidal neovascularization [PDF]
AIM: To investigate the clinical characteristics and genetic features of a Bietti crystalline dystrophy (BCD) proband in a Chinese family. METHODS: A Chinese female diagnosed with BCD complicated by bilateral choroidal neovascularization (CNV) and her ...
Xin-Yao Han +5 more
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Infrared imaging enhances retinal crystals in Bietti’s crystalline dystrophy
Vikram S Brar, William H Benson Department of Ophthalmology, Medical College of Virginia Campus, Virginia Commonwealth University School of Medicine, Richmond, VA, USA Abstract: Infrared imaging dramatically increased the number of crystalline ...
Brar VS, Benson WH
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Novel CYP4V2 mutations associated with Bietti crystalline corneoretinal dystrophy in Chinese patients [PDF]
AIM: To analyze the CYP4V2 mutations in five unrelated Chinese patients with Bietti crystalline corneoretinal dystrophy (BCD) and to provide clinical features of these patients.
Rong Tian +3 more
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Spectral Domain Optical Coherence Tomographic Findings of Bietti Crystalline Dystrophy [PDF]
We analyzed the OCT features of 24 eyes of 12 patients with Bietti crystalline dystrophy (BCD) with the Heidelberg HRA2-OCT. Seventeen of 24 eyes were in intermediate stage of the disease and seven in advanced stage of the disease at the time of latest ...
Ali Osman Saatci +3 more
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Molecular analysis and phenotypic study in 14 Chinese families with Bietti crystalline dystrophy. [PDF]
To investigate the clinical features and cytochrome P450 family 4 subfamily V polypeptide 2 (CYP4V2) gene mutations in 14 Chinese families with Bietti crystalline dystrophy (BCD).Seventeen patients from 14 unrelated Chinese families with BCD were ...
Houfa Yin +9 more
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Evolution of Cellular Inclusions in Bietti’s Crystalline Dystrophy
Bietti’s crystalline dystrophy (BCD) consists of small, yellow-white, glistening intraretinal crystals in the posterior pole, tapetoretinal degeneration with atrophy of the retinal pigment epithelium (RPE) and “sclerosis” of the choroid; in addition ...
Emiko Furusato +2 more
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