Results 81 to 90 of about 595 (159)

Spectral Domain Optical Coherence Tomographic Findings of Bietti Crystalline Dystrophy

, 2020
We analyzed the OCT features of 24 eyes of 12 patients with Bietti crystalline dystrophy (BCD) with the Heidelberg HRA2-OCT. Choroidal hyperreflective spots were noted in 21 of 24 eyes (87.5%).
Ali Osman Saatci, Aylin Yaman, Hasan Can Doruk, Ferit Hakan Öner   +3 more
core  

Clinical and genetic features in Italian Bietti crystalline dystrophy patients

, 2013
AIM: The aim of the study was to describe the clinical and genetic features of 15 Italian patients with Bietti crystalline dystrophy (BCD). METHODS: All study participants underwent a complete ophthalmological examination, including standard ...
ROSSI, Settimio, Li A, SIMONELLI, Francesca, Gesualdo C, TESTA, Francesco, Hejtmancik JF, Yaylacioğlu F   +6 more
core   +1 more source

Longitudinal structure-function analysis of molecularly-confirmed CYP4V2 Bietti Crystalline Dystrophy [PDF]

, 2023
Objectives: Bietti Crystalline Dystrophy (BCD) is an autosomal recessive progressive retinal disease caused by mutations in CYP4V2. We have characterised the natural history including structural and functional measures to identify potential outcome ...
Moosajee, Mariya, Clough, Neil, Jackson, Daniel, Cheloni, Riccardo   +3 more
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Outer retinal circular structures in patients with Bietti crystalline retinopathy. [PDF]

, 2011
[Background] : Bietti crystalline retinopathy (BCR) is a distinct retinal degenerative disease characterised by retinal degeneration with many yellow–white crystals located mainly at the posterior pole area.
Makiyama, Yukiko, Nakagawa, Satoko, Satoko Nakagawa, Guo, Congrong, Otani, Atsushi, Ogino, Ken, Masafumi Kurimoto, Ken Ogino, Yoshimura, Nagahisa, Congrong Guo, Atsushi Otani, Hiroshi Kojima, Nagahisa Yoshimura, Kurimoto, Masafumi, Kojima, Hiroshi, Yukiko Makiyama   +15 more
core   +1 more source

Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2

, 2004
Bietti crystalline corneoretinal dystrophy (BCD) is an autosomal recessive retinal dystrophy characterized by multiple glistening intraretinal crystals scattered over the fundus, a characteristic degeneration of the retina, and sclerosis of the choroidal
Iwata, Fumino, Jiao, Xiaodong, Kaiser-Kupfer, Muriel, Alan Lewis, Richard, Hejtmancik, J. Fielding, Zhang, Qingjiong, Traboulsi, Elias I., Sergeev, Yuri V., Schorderet, Daniel F., Munier, Francis L., Shy Chen, Muh, Hayakawa, Mutsuko, Xiao, Xueshan, Heckenlively, John, Li, Anren, Kanai, Atsushi, Weleber, Richard G., Yao, Wenliang   +17 more
core   +1 more source

Choroidal vasculature in bietti crystalline dystrophy with CYP4V2 mutations and in retinitis pigmentosa with EYS mutations [PDF]

, 2017
Purpose: We compare the choroidal vascular area between Bietti crystalline dystrophy (BCD) patients with CYP4V2 mutations, retinitis pigmentosa (RP) patients with EYS mutations, and normal controls, and investigate the correlation between choroidal ...
Ishihara, Kenji, Yoshikawa, Munemitsu, 黒田, 能匡, 宮田, 学, 畑, 匡侑, Sugahara, Masako, Hata, Masayuki, 石原, 健司, Ooto, Sotaro, 吉村, 長久, Miyata, Manabu, 長谷川, 智子, Hirashima, Takako, 菅原, 麻紗子, Ogino, Ken, Muraoka, Yuki, Yoshimura, Nagahisa, Hasegawa, Tomoko, 平島, 貴子, 吉川, 宗光, 荻野, 顕, Kuroda, Yoshimasa, 大音, 壮太郎, 村岡, 勇貴   +23 more
core   +2 more sources

Evolution of Cellular Inclusions in Bietti’s Crystalline Dystrophy

Ophthalmology and Eye Diseases, 2010
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, sparking yellow crystals in the superficial marginal cornea are also found in many patients.
Emiko Furusato, J. Douglas Cameron, Chi-Chao Chan   +2 more
openaire   +3 more sources

A Novel Compound Heterozygous Mutation in the CYP4V2 Gene in a Japanese Patient with Bietti’s Crystalline Corneoretinal Dystrophy

Case Reports in Ophthalmology, 2011
Purpose: To describe the clinical and genetic characteristics of a Japanese family in which one member exhibited Bietti’s crystalline corneoretinal dystrophy (BCD).
Yumiko Yokoi, Kota Sato, Hajime Aoyagi, Yoshihisa Takahashi, Minako Yamagami, Mitsuru Nakazawa   +5 more
doaj   +1 more source

Genetic Linkage of Bietti Crystallin Corneoretinal Dystrophy to Chromosome 4q35

, 2000
Bietti crystalline corneoretinal dystrophy (BCD) is an autosomal recessive retinal degeneration characterized by multiple glistening intraretinal dots scattered over the fundus, degeneration of the retina, and sclerosis of the choroidal vessels ...
Iwata, Fumino, Schorderet, Daniel F., Jiao, Xiaodong, Munier, Francis L., Kaiser-Kupfer, Muriel, Hayakawa, Mutsuko, Hejtmancik, J. Fielding, Chen, Muh-Shy, Lee, June, Kanai, Atsushi   +9 more
core   +1 more source

Choroidal thickness profile in inherited retinal diseases in Indian subjects

Indian Journal of Ophthalmology, 2015
Purpose: To evaluate changes in choroidal thickness (CT) in inherited retinal diseases and its relationship with age, spherical equivalent, visual acuity, and macular thickness.
Jay Chhablani, Ashraya Nayaka, Padmaja Kumari Rani, Subhadra Jalali   +3 more
doaj   +1 more source