Combination of Trabeculectomy and Primary Pars Plana Vitrectomy in the Successful Treatment of Angle-Closure Glaucoma with BEST1 Mutations: Self-Controlled Case Series
Author:
Publisher
Springer Science and Business Media LLC
Subject
Ophthalmology
Link
https://link.springer.com/content/pdf/10.1007/s40123-022-00580-1.pdf
Reference19 articles.
1. Burgess R, Millar ID, Leroy BP, et al. Biallelic mutation of BEST1 causes a distinct retinopathy in humans. Am J Hum Genet. 2008;82(1):19–31.
2. Boon CJ, van den Born LI, Visser L, et al. Autosomal recessive bestrophinopathy: differential diagnosis and treatment options. Ophthalmology. 2013;120(4):809–20.
3. Luo J, Lin M, Guo X, et al. Novel BEST1 mutations and special clinical characteristics of autosomal recessive bestrophinopathy in Chinese patients. Acta Ophthalmol. 2019;97(3):247–59.
4. Casalino G, Khan KN, Armengol M, et al. Autosomal recessive bestrophinopathy: clinical features, natural history, and genetic findings in preparation for clinical trials. Ophthalmology. 2021;128(5):706–18.
5. Xuan Y, Zhang Y, Zong Y, et al. The clinical features and genetic spectrum of a large cohort of Chinese patients with vitelliform macular dystrophies. Am J Ophthalmol. 2020;216:69–79.
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