نتایج جستجو برای: corneal dystrophy

تعداد نتایج: 48915  

In the current study, we conducted a mutation screening of tumor-associated calcium signal transducer 2 (TACSTD2) gene in six consanguineous Iranian families with gelatinous drop-like corneal dystrophy (GDLD), in order to find the causative mutations. Detailed eye examination was performed by ophthalmologist to confirm GDLD in patients. To detect the possible mutations, direct Sanger sequencing...

A SHarifi S Ahmadi

Background & Aims: This study was carried out to determine the leading indications for corneal transplantation in Kerman province. Methods: Medical records of 186 patients underwent corneal transplantation during 3 years (2004-2006) in Shafa Medical Center were evaluated retrospectively. The initial diagnosis and causes of corneal grafting were recorded. Infectious keratitis (Bacterial, Fungal,...

Journal: :بینا 0
محمدرضا سلیمانی mr soleimani دانشگاه علوم پزشکی رفسنجان محمدعلی جوادی ma javadi تهران- پاسداران- بوستان نهم- بیمارستان لبافی نژاد- مرکز تحقیقات چشم محمد زارع m zare تهران- پاسداران- بوستان نهم- بیمارستان لبافی نژاد- مرکز تحقیقات چشم علی شریفی a sharifee دانشگاه علوم پزشکی کرمان

purpose: to evaluate changes in indications of corneal transplantation at labbafinejad medical center during 2001-2003. methods: records of 563 from 684 patients who had undergone corneal transplantation from oct. 2001 to oct. 2003 were evaluated. all the procedures were performed by corneal surgeons and fellows. findings: there were 292 male (51.9%) and 217 female (48.1%) subjects ranging in a...

Journal: :journal of current ophthalmology 0
محمدحسین داوری mohammad-hossein davari عبدا... امینی abdullah amini

purpose : the aim of this study was to determine indications of keratoplasty during 7 years (1999–2006) in emam-rreza and vali-asr teaching hospitals of birjand university of medical sciences. methods : medical records of all patients who underwent penetrating keratoplasty (pk) in teaching hospitals of birjand university of medical sciences from 1999 to 2006 were investigated retrospectively. t...

Journal: :Frontiers in bioscience : a journal and virtual library 2003
Gordon K Klintworth

The pertinent literature on inherited corneal diseases is reviewed in terms of the chromosomal localization and identification of the responsible genes. Disorders affecting the cornea have been mapped to human chromosome 1 (central crystalline corneal dystrophy, familial subepithelial corneal amyloidosis, early onset Fuchs dystrophy, posterior polymorphous corneal dystrophy), chromosome 4 (Biet...

Journal: :بینا 0
محمدعلی جوادی ma javadi ophthalmic research center, shahid beheshti university of medical sciences, tehran, iranمرکز تحقیقات چشم- دانشگاه علوم پزشکی شهید بهشتی- تهران- ایران سپهر فیضی s feizi مرکز تحقیقات چشم- دانشگاه علوم پزشکی شهید بهشتی- تهران- ایران رویا جعفری r jafari مرکز تحقیقات چشم- دانشگاه علوم پزشکی شهید بهشتی- تهران- ایران فیروز میربابایی f mirbabaee تهران- پاسداران- بوستان نهم- خیابان پایدارفرد (خیابان امیر ابراهیمی)- پلاک 23- مرکز تحقیقات چشم

purpose: to compare clinical and confocal scan outcomes after descemet stripping automated endothelial keratoplasty (dsaek) performed for fuchs’ endothelial dystrophy versus pseudophakic bullous keratopathy. methods: in this retrospective comparative study, 47 consecutive eyes of 39 patients with the diagnosis of fuchs’ endothelial dystrophy (n=29, group 1) or pseudophakic bullous keratopathy (...

Journal: :Investigative ophthalmology & visual science 2011
David C Musch Leslie M Niziol Joshua D Stein Roheena M Kamyar Alan Sugar

PURPOSE To estimate the prevalence of corneal dystrophies. METHODS Records of almost 8 million enrollees in a national managed-care network throughout the United States who had an eye care visit in 2001 to 2009 were searched for a recording of corneal dystrophy on a claim submitted by an ophthalmologist or optometrist from January 1, 2001, through December 31, 2007. RESULTS Unique individua...

Journal: :The British journal of ophthalmology 2000
C Akimune H Watanabe N Maeda M Okada S Yamamoto A Kiritoshi Y Inoue Y Shimomura Y Tano

AIMS To investigate the frequency of corneal guttata in patients with a corneal dystrophy resulting from an Arg124His (R124H) mutation of betaig-h3 gene. METHODS Slit lamp examination was performed on 30 eyes with corneal dystrophy from a genetically confirmed betaig-h3 R124H mutation and on 50 age matched control eyes. The stage of the corneal dystrophy was classified as stage 0, I, or II an...

Journal: :Cornea 2015
Jayne S Weiss Hans Ulrik Møller Anthony J Aldave Berthold Seitz Cecilie Bredrup Tero Kivelä Francis L Munier Christopher J Rapuano Kanwal K Nischal Eung Kweon Kim John Sutphin Massimo Busin Antoine Labbé Kenneth R Kenyon Shigeru Kinoshita Walter Lisch

PURPOSE To update the 2008 International Classification of Corneal Dystrophies (IC3D) incorporating new clinical, histopathologic, and genetic information. METHODS The IC3D reviewed worldwide peer-reviewed articles for new information on corneal dystrophies published between 2008 and 2014. Using this information, corneal dystrophy templates and anatomic classification were updated. New clinic...

Journal: :Arquivos brasileiros de oftalmologia 2012
Elvira Barbosa Abreu Gustavo Amorin Novaes Bruno Franco Fernandes Patricia Rusa Pereira Odashiro Alexandre Nakao Odashiro Isabella de Oliveira Lima Parizotto Miguel Noel Burnier

INTRODUCTION Corneal dystrophy is defined as bilateral and symmetric primary corneal disease, without previous associated ocular inflammation. Corneal dystrophies are classified according to the involved corneal layer in superficial, stromal, and posterior dystrophy. Incidence of each dystrophy varies according to the geographic region studied. PURPOSE To evaluate the prevalence of stromal co...

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