RETINAL DETACHMENT IN A PATIENT WITH LEBER CONGENITAL AMAUROSIS
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Ophthalmology,General Medicine
Reference10 articles.
1. Centrosomal-ciliary geneCEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosis
2. Leber Congenital Amaurosis–A Model for Efficient Genetic Testing of Heterogeneous Disorders: LXIV Edward Jackson Memorial Lecture
3. Tractional retinal detachment in Usher syndrome type II
4. Retinal Detachment and Retinal Holes in Retinitis Pigmentosa Sine Pigmento
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1. Clinical and Molecular Features of a Chinese Cohort With Syndromic and Nonsyndromic Retinal Dystrophies Related to the CEP290 Gene;American Journal of Ophthalmology;2023-04
2. Retinal detachment in a child with severe early childhood onset retinal dystrophy;BMJ Case Reports;2018-08-27
3. Noninfectious Endophthalmitis after Intravitreal Injection of Aflibercept;Journal of the Korean Ophthalmological Society;2016
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