نتایج جستجو برای: iridocorneal endothelial syndrome

تعداد نتایج: 746121  

Journal: :Acta ophthalmologica Scandinavica 2006
Paul Dighiero Sébastien Guigou Martial Mercie Benoit Briat Pierre Ellies Jean-Jacques Gicquel

PURPOSE To present a new surgical technique combining penetrating keratoplasty and open-sky posterior iris fixation of the Artisan iris-claw intraocular lens (IOL) for treatment of pseudophakic bullous keratopathy in a case series of five patients. METHODS A graft diameter of 8.25 mm was chosen. The formerly implanted angle-supported IOL was removed. The IOL was enclosed, entrapping a fractio...

Journal: :Human molecular genetics 2010
Markus Kroeber Noa Davis Silvia Holzmann Michaela Kritzenberger Michal Shelah-Goraly Ron Ofri Ruth Ashery-Padan Ernst R Tamm

Heterozygous mutations in PAX6 are causative for aniridia, a condition that is frequently associated with juvenile glaucoma. Defects in morphogenesis of the iridocorneal angle, such as lack of trabecular meshwork differentiation, absence of Schlemm's canal and blockage of the angle by iris tissue, have been described as likely causes for glaucoma, and comparable defects have been observed in he...

2013
Sang Beom Han Hengpei Ang Deepa Balehosur Gary Peh Shyam S. Chaurasia Donald T. H. Tan Jodhbir S. Mehta

PURPOSE To develop a mouse model of bullous keratoplasty and evaluate the safety and efficacy of cryoinjury-induced corneal endothelial decompensation. METHODS Transcorneal freezing was performed on the right eye of each mouse. One cycle of cryoinjury was performed in 18 eyes (group A), and three cycles were performed in 17 eyes (group B). Pachymetry and intraocular pressure (IOP) measurement...

Journal: :Nepalese journal of ophthalmology : a biannual peer-reviewed academic journal of the Nepal Ophthalmic Society : NEPJOPH 2015
B Satana C Altan B Basarir Z Alkin O F Yilmaz

BACKROUND We describe a patient with microspherophakia due to Weill-Marchesani syndrome accompanied by developmental angle anomaly who was successfully treated with a surgery of combined PPL and goniotomy. CASE We report ocular findings of a 1-year-old girl who was diagnosed with Weill-Marchesani syndrome with a positive family history of glaucoma in her cousins and glaucoma with anterior seg...

2015
Hee Jung Yang You Kyung Lee Choun-Ki Joo Jung Il Moon Jee Won Mok Myoung Hee Park

PURPOSE To describe clinical findings in a Korean family with Axenfeld-Rieger syndrome. METHODS A retrospective review of clinical data about patients with diagnosed Axenfeld-Rieger syndrome. Five affected members of the family underwent a complete ophthalmologic examination. We screened the forkhead box C1 gene and the pituitary homeobox 2 gene in patients. Peripheral blood leukocytes and bu...

رسمی , یوسف, خادم انصاری, محمدحسن , ولی پور , فریبا , ولیزاده , ندا ,

    Background & Aims : The metabolic syndrome (MS) is a clustering of risk factors of metabolic origin that increases the risk for cardiovascular disease . Endothelial function biomarkers and lipids profile determine cardiovascular disease . Aim of this study was to investigate the effect of sex on endothelial function and lipid profile.   Materials & M ethods: The present study involved 77 pa...

2013
Matthew T Whitehead Asim F Choudhri Sarwat Salim

Axenfeld-Rieger syndrome (ARS) is a genetic disorder representing a disease spectrum resulting from neural crest cell maldevelopment. Glaucoma is a common complication from the incomplete formation of the iridocorneal angle structures. Neural crest cells also form structures of the forebrain and pituitary gland, dental papillae, aortic arch walls, genitalia, and long bones; therefore, patients ...

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