نتایج جستجو برای: corneal deposits

تعداد نتایج: 56615  

2004
F. C. RODGER

A report of a woman in her fifties with Schnyder's crystalline stromal dystrophy is presented. There is no personal or family history of hypercholesterolaemia. A full thickness corneal disc was removed before grafting and examined by polarised light, histochemistry, and electron microscopy. Specific lipid histochemical methods showed deposits of cholesterol and cholesterol ester in the superfic...

Journal: :journal of current ophthalmology 0
سیدمنصور رضوی seyed mansour razavi پیمان سلامتی peyman salamati سپهر فیضی sepehr feizi محمدعلی جوادی mohammad ali javadi

purpose : to review ocular surface abnormalities caused by exposure to mustard gas and current approaches to manage its delayed-onset complications methods : a total of 198 medical articles related to mustard gas were reviewed using known international medical databases, 114 articles were more relevant to the main aim were selected. results : mustard gas-related ocular injuries can be divided i...

Journal: :medical hypothesis, discovery and innovation ophthalmology journal 0
ali osman saatci department of ophthalmology, dokuz eylul university, izmir, turkey hasan can doruk department of ophthalmology, dokuz eylul university, izmir, turkey

bietti’s crystalline dystrophy (bcd) is a rare disease presenting with the appearance of intraretinal crystalline deposits and varying degrees of chorioretinal atrophy commencing at the posterior pole. within time, intraretinal crystals gradually disappear and chorioretinal atrophy extends beyond the macula even resulting in complete chorioretinal atrophy. concomitant corneal crystals can be ...

Journal: :Investigative ophthalmology & visual science 1995
C Verhagen T Rowshani B Willekens N J van Haeringen

PURPOSE The presence of corneal opacities associated with dacryoadenitis and lacrimal gland destruction has led investigators to consider MRL/Mp mice as models for band keratopathy and Sjögren syndrome. In this study, the authors examined the time course of the corneal opacification and investigated whether the opacities were associated with altered serum levels of parathyroid hormone, calcium,...

Journal: :Arquivos brasileiros de oftalmologia 2007
Gustavo Victor Milton Ruiz Alves Walton Nosé

PURPOSE To describe in vivo confocal microscopy findings in patients with different stages of amiodarone-induced keratopathy, and correlate biomicroscopy stages with confocal stages. METHODS Twenty eyes of 10 patients (6 men and 4 women), who receive treatment with amiodarone were selected for the study with confocal microscopy (MC). RESULTS The average age was 58 +/- 6.2 years (50-66 years...

Journal: :The British journal of ophthalmology 1998
M Yamada H Mochizuki Y Kamata Y Nakamura Y Mashima

AIM To report the quantitation of the lipid composition of a corneal button from a Japanese woman in her 60s with clinically and histopathologically proved Schnyder's corneal dystrophy. METHODS Total lipids extracted from the corneal button of the patient were analysed by the method of thin layer chromatography flame ionisation detection. Two different solvent systems were used for neutral li...

Journal: :Investigative ophthalmology & visual science 1998
W W Kao C W Kao A H Kaufman K W Kombrinck R L Converse W V Good T H Bugge J L Degen

PURPOSE The local deposition of fibrinogen and other plasma products from tears within corneal wounds and the expression of plasminogen activator by corneal epithelial cells suggest that the coagulation and fibrinolytic systems play an important role in corneal wound healing. The authors used mouse lines deficient in plasminogen (Plg), fibrinogen (Fib), or both to elucidate the roles of these k...

Journal: :Investigative ophthalmology & visual science 2002
Mohamed F El-Ashry Mai M Abd El-Aziz Simon Wilkins Michael E Cheetham Susan E Wilkie Alison J Hardcastle Stephanie Halford Ahmed Y Bayoumi Linda A Ficker Stephen Tuft Shomi S Bhattacharya Neil D Ebenezer

PURPOSE Macular corneal dystrophy (MCD) is a rare corneal dystrophy that is characterized by abnormal deposits in the corneal stroma, keratocytes, Descemet's membrane, and endothelium, accompanied by progressive clouding. It has been classified into three immunophenotypes--MCD types I, IA, and II--according to the serum level of sulfated keratan sulfate (KS) and immunoreactivity of the corneal ...

Journal: :Investigative ophthalmology & visual science 2004
Gordon K Klintworth Wenjun Bao Natalie A Afshari

PURPOSE To determine the genetic basis for lattice corneal dystrophy (LCD) in an extensively studied family. METHODS Ten affected family members were examined clinically, and three individuals were studied with in vivo confocal microscopy and optical coherence tomography (OCT). Corneal tissues from eight affected family members were examined histopathologically. The status of the transforming...

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