Zobrazeno 1 - 10
of 298
pro vyhledávání: '"FEVR"'
Autor:
Liam D. Redden, Douglas S.M. Iaboni, Sarah van der Ende, Mathew Nightingale, Daniel Gaston, Christopher R. McMaster, Johane M. Robitaille, R. Rishi Gupta
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 34, Iss , Pp 102051- (2024)
Purpose: To report a rare clinical finding of preretinal granules associated with atypical familial exudative vitreoretinopathy (FEVR) and perform a review of the literature. Observations: An asymptomatic 18-year-old male was referred for unilateral
Externí odkaz:
https://doaj.org/article/f431d01d49954f5086b1f69028654a4a
Autor:
Sadık Etka Bayramoğlu, Nihat Sayın, Mehmet Erdoğan, Sümeyra Doğan, Alper Gezdirici, Merih Çetinkaya
Publikováno v:
Türk Oftalmoloji Dergisi, Vol 53, Iss 6, Pp 386-389 (2023)
A female infant born with a gestational age of 35 weeks and birth weight of 2500 g was referred for ophthalmic examination on the second postnatal day. Bilateral venous dilatation and arterial tortuosity, severe extraretinal fibrovascular proliferati
Externí odkaz:
https://doaj.org/article/82dec6b0b8ec4258bdfeb805a527f39d
Autor:
Jiayu Li, Chanjuan Wang, Shaochi Zhang, Bo Cai, Bo Pan, Caihong Sun, Xiaolong Qi, Chunmei Ma, Wei Fang, Kangxin Jin, Xiaojun Bi, Zibing Jin, Wenjuan Zhuang
Publikováno v:
BMC Ophthalmology, Vol 23, Iss 1, Pp 1-19 (2023)
Abstract Background Familial exudative vitreoretinopathy (FEVR) is a genetic eye disorder that leads to abnormal development of retinal blood vessels, resulting in vision impairment. This study aims to identify pathogenic variants by targeted exome s
Externí odkaz:
https://doaj.org/article/1b581b4cf8fe48d6b703279fbf268c52
Publikováno v:
Orthopedic Research and Reviews, Vol Volume 15, Pp 39-45 (2023)
Jake Littman,1 Chanika Phornphutkul,2 Celine Saade,3 Julia Katarincic,1 Roy Aaron1 1Department of Orthopedic Surgery, Warren Alpert Medical School of Brown University, Providence, RI, USA; 2Division of Human Genetics, Department of Pediatrics, Hasbro
Externí odkaz:
https://doaj.org/article/ff326069353b4e159eac1443db412b08
Akademický článek
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Akademický článek
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Publikováno v:
BMC Ophthalmology, Vol 22, Iss 1, Pp 1-11 (2022)
Abstract Purpose To describe and analyze the clinical prognosis of infants diagnosed of familial exudative vitreoretinopathy (FEVR) with single gene mutation in long-term follow-up. Methods A retrospective case study was conducted on 355 FEVR infants
Externí odkaz:
https://doaj.org/article/629ae9d4cda3478d9d6a9e67486ae5cd
Publikováno v:
International Journal of Retina and Vitreous, Vol 8, Iss 1, Pp 1-6 (2022)
Abstract Background Familial Exudative Vitreoretinopathy (FEVR) is a hereditary disorder characterized by peripheral avascular retina with neovascularization. Although FEVR has been thoroughly described in multiple literature publications from differ
Externí odkaz:
https://doaj.org/article/3609f54e52114ca48d118d67cd2f7daa
Autor:
Vincent Le, Gabrielle Abdelmessih, Wendy A. Dailey, Cecille Pinnock, Victoria Jobczyk, Revati Rashingkar, Kimberly A. Drenser, Kenneth P. Mitton
Publikováno v:
Cells, Vol 12, Iss 21, p 2579 (2023)
Familial Exudative Vitreoretinopathy (FEVR), Norrie disease, and persistent fetal vascular syndrome (PFVS) are extremely rare retinopathies that are clinically distinct but are unified by abnormal retinal endothelial cell function, and subsequent irr
Externí odkaz:
https://doaj.org/article/44991ceb75bd4bf8b93a721d0f849f71
Autor:
Vishal Agrawal, Sonal Kalia
Publikováno v:
Indian Journal of Ophthalmology, Vol 70, Iss 7, Pp 2490-2496 (2022)
Purpose: To report the clinical profile, management, and long-term anatomical and visual acuity (VA) outcomes of pediatric macula-off rhegmatogenous retinal detachment (RRD) secondary to familial exudative vitreoretinopathy (FEVR). Methods: This was
Externí odkaz:
https://doaj.org/article/b1e7ed2b771e4fd0948227dcf18f1528