نتایج جستجو برای: leber’s congenital amaurosis

تعداد نتایج: 120868  

پایان نامه :دانشگاه آزاد اسلامی واحد علوم پزشکی تهران - دانشکده پزشکی 1390

هدف: این مطالعه به منظور بررسی میزان فراوانی بیماری lebers congenital amaurosis در تست های الکتروفیزیولوژیک در کودکان در پلی کلینیک قدس سال 90-89 انجام شده است. روش مطالعه: در این مطالعه مقطعی، 50 فرد بدون وجود سابقه اختلال بینایی و تشنج وارد مطالعه شدند شامل 25 نفر مبتلا به lebers congenital amaurosis و 25 نفر که سالم و بعنوان گروه شاهد بودند. دو گروه تحت erg و vep و eog قرار گرفتند و نتایج ب...

2005
E Samaila

Retinitis pigmentosa (RP) is the generic name for a group of hereditary disorders characterized by progressive loss of photoreceptors and RPE function. The classical triad of retinitis pigmentosa is arteriolar attenuation, retinal bone spicule pigmentation and waxy disc pallor. Lebers congenital amaurosis (LCA) is the hereditary form of retinitis pigmentosa. It presents with blindness either at...

Journal: :Nigerian Journal of Ophthalmology 2008

Journal: :British Journal of Ophthalmology 1985

Journal: :journal of current ophthalmology 0
مرتضی مواسات morteza movassat رامک روحی پور ramak roohipour مهدی نیلی احمدآبادی mehdi nili-ahmadabadi

purpose : to evaluate the incidence of leber’s congenital amaurosis (lca) in low vision children referred to electrophysiology ward of farabi eye hospital , and review the clinical features of disease and electroretiongraphy (erg) test values to confirm the diagnosis and severity of the disease in iran . design: prospective observational case series methods : two-hundred and fifteen cases of lo...

2014
Caterina Ripamonti G. Bruce Henning Robin R. Ali James W. Bainbridge Scott J. Robbie Venki Sundaram Vy A. Luong L. Ingeborgh van den Born Ingele Casteels Thomy J. L. de Ravel Anthony T. Moore Andrew Stockman

Citation: Ripamonti C, Henning GB, Ali RR, et al. Nature of the visual loss in observers with Leber’s congenital amaurosis caused by specific mutations in RPE65. Invest Ophthalmol Vis Sci. 2014;55:6817–6828. DOI: 10.1167/iovs.14-14923 PURPOSE. To characterize visual losses associated with genetic mutations in the RPE65 gene that cause defects in the RPE-specific isomerase, RPE65. RPE65 is an im...

Journal: :Molecular vision 2003
Carlo Rivolta Radha Ayyagari Paul A Sieving Eliot L Berson Taddeus P Dryja

PURPOSE To determine whether pathogenic mutations exist in the ELOVL4 gene in patients with inherited retinal degenerations other than Stargardt-like macular dystrophy or other hereditary macular degenerations. METHODS All six exons comprising the open reading frame of the ELOVL4 gene were evaluated by single-strand conformation analysis, direct nucleotide sequencing, or both methods. RESUL...

Journal: :The British journal of ophthalmology 1985
H Skalka

rig. renpheralfundus cS. We have had occasion to see a similar case, first in 1974 when the patient, a black female with no apparent vision but otherwise well, was 6 months old. At that time dilated fundus examination under anaesthesia (EUA) was normal. Repeat EUA in 1977 at age 4 years revealed bilateral peripheral fundus lesions essentially identical to those described by Chew et al. (Figs. 1...

Journal: :Clinical genetics 2013
A Kaur

1. Weleber RG, Francis PJ, Trzupek KM. Leber ongenital amaurosis 2004 [Updated 2010]. In: Pagon RA, Bird TD, Dolan CR, et al., eds. GeneReviewsTM [Internet] (WA): University of Washington, 1993, from: http://www.ncbi.nlm.nih.gov/books/NBK1298/ 2. Bainbridge JW, Smith AJ, Barker SS et al. Effect of gene therapy on visual function in Leber’s congenital amaurosis. N Engl J Med 2008: 358 (21): 2231...

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