Zobrazeno 1 - 10
of 265
pro vyhledávání: '"Best vitelliform macular dystrophy"'
Publikováno v:
Guoji Yanke Zazhi, Vol 24, Iss 7, Pp 1147-1151 (2024)
AIM: To observe the multimodal imaging characteristics of Best vitelliform macular dystrophy(BVMD).METHODS:The clinical data of 30 patients(60 eyes)diagnosed as BVMD at stage Ⅰ to Ⅳ in Nanjing Medical University Affiliated Eye Hospital from June
Externí odkaz:
https://doaj.org/article/219d579cef714613a16ef1db21f255f9
Publikováno v:
Guoji Yanke Zazhi, Vol 23, Iss 11, Pp 1920-1924 (2023)
AIM: To observe the multimodal image features of dome-shaped macula(DSM)with subretinal fluid(SRF)in adolescents with high myopia, and investigate its typical features and identification methods.METHODS: This is a retrospective study. A total of 21 a
Externí odkaz:
https://doaj.org/article/f4072b7410e94826b7e4ccab8bad516d
Autor:
Lorenzo Bianco, MD, Alessandro Arrigo, MD, PhD, Alessandro Marchese, MD, Alessio Antropoli, MD, Emanuela Aragona, MD, PhD, Lamberto La Franca, MD, Luca Mauro, MD, Adelaide Pina, MsC, Rashid Hassan Farah, MsC, Giulia Basile, MsC, Francesco Bandello, MD, FEBO, Maurizio Battaglia Parodi, MD
Publikováno v:
Ophthalmology Science, Vol 3, Iss 4, Pp 100329- (2023)
Purpose: To analyze fixation location and stability in best vitelliform macular dystrophy (BVMD) and test their association with best-corrected visual acuity (BCVA). Design: Observational, cross-sectional study. Participants: Thirty patients (55 eyes
Externí odkaz:
https://doaj.org/article/1c233c850f064a649d5e22d6bdc4c551
Publikováno v:
BMC Ophthalmology, Vol 23, Iss 1, Pp 1-6 (2023)
Abstract Background Best vitelliform macular dystrophy (BVMD), caused by pathogenic variants of the BEST1 gene, has not been reported in association with cataracts and ocular malformations. We reported a case with a complex ocular phenotype comprisin
Externí odkaz:
https://doaj.org/article/40cdd9346faf45f9a16a6dd1e84928cf
Autor:
N. V. Matcko, M. V. Gatsu
Publikováno v:
Acta Biomedica Scientifica, Vol 7, Iss 1, Pp 74-81 (2022)
Background. Vitelliform dystrophies, first detected in adulthood, may create complications in diagnosis, especially with partial or almost complete destruction of vitelliform material, disguising as various types of macular pathology, such as central
Externí odkaz:
https://doaj.org/article/7745a046b2194f0499aa15bd04cf1c4a
Autor:
Zhi-Hong Zhu, Xin Jin, Yi-Xin Zhang, Rui Wang, Tong Wu, Wei Liu, Ze-Hua Chen, Hai-Nan Xie, Lan-Lan Chen, Zi-Hao Liu, Hou-Bin Huang
Publikováno v:
International Journal of Ophthalmology, Vol 15, Iss 2, Pp 205-212 (2022)
AIM: To describe the clinical heterogeneity of patients with novel mutations in BEST1. METHODS: All the members in the two Chinese families underwent detailed clinical evaluations including best-corrected visual acuity, slit-lamp examination, applana
Externí odkaz:
https://doaj.org/article/c30fb6bbf0b741d4921de97976ebb02b
Autor:
Srikanta Kumar Padhy, Deepika C Parameswarappa, Komal Agarwal, Brijesh Takkar, Shashwat Behera, Bhavik Panchal, Muralidhar Ramappa, Tapas Ranjan Padhi, Subhadra Jalali
Publikováno v:
Indian Journal of Ophthalmology, Vol 70, Iss 7, Pp 2516-2525 (2022)
Purpose: To evaluate patterns of pediatric vitelliform macular dystrophy (PVMD). Methods: This is a retrospective analysis of Indian children with vitelliform macular dystrophy (VMD) presenting within the first decade of life. Records were evaluated
Externí odkaz:
https://doaj.org/article/916a185a1761431f877447fc3ffbb069
Autor:
Shangying Yang, Zhen Li, Wanyu Cheng, Meijiao Ma, Rui Qi, Xue Rui, Yinghua Ren, Xunlun Sheng, Weining Rong
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 1, Pp n/a-n/a (2023)
Abstract Purpose To report novel BEST1 variants in six Chinese families with bestrophinopathies of two different inheritance modes and analyze the intrafamilial phenotypic diversity. Method A total of 25 participants including 13 patients and 12 heal
Externí odkaz:
https://doaj.org/article/53af159aed1e43af88aa48a24c15d6ed
Akademický článek
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Autor:
Jale Menteş, Mine Esen Barış
Publikováno v:
Türk Oftalmoloji Dergisi, Vol 51, Iss 3, Pp 188-191 (2021)
This case report of a 38-year-old man with bilateral Best vitelliform macular dystrophy (BVMD) presents bilateral quiescent type 1 neovascularizations (NV) detected by optical coherence angiography (OCTA) and their multimodal imaging characteristics.
Externí odkaz:
https://doaj.org/article/81b989425a3f406d84745ab05428aca7