نتایج جستجو برای: corneal deposits

تعداد نتایج: 56615  

2010
Cinthya Ramos-Castellón Gabriela Ortiz-Nieva Fernando Fresán Leonardo Villalvazo Yonathan Garfias Alejandro Navas María C. Jiménez-Martínez

A 43-year-old man with linear immunoglobulin A (IgA) dermatosis associated with gluten intolerance presented with progressive vision loss, pain and photosensitivity in both eyes. His visual acuity was light perception (LP) in both eyes. A physical examination revealed bullous, papular lesions with erythematous borders in periocular tissues, limbs, and thorax. Slit-lamp examination showed conjun...

Journal: :The British journal of ophthalmology 1970
J A Caldeira E Sabbaga L E Ianhez

Secondary calcareous degeneration of the conjunctiva or cornea may follow such pathological conditions of the eye as spring catarrh, erysipelas of the lids, leucomata, uveitis, trauma, etc. On the other hand, primary calcareous degeneration is rare (Duke-Elder and Leigh, I965); the corneal deposits occur on Bowman's membrane and the superficial layers of the stroma, acting as foreign bodies and...

Journal: :The Journal of general virology 2006
Naoyuki Morishige James V Jester Julie Naito Nelson Osorio Andrew Wahlert Clinton Jones Roger D Everett Steven L Wechsler Guey Chuen Perng

Herpes stromal keratitis (HSK) results from the reactivation of herpes simplex virus type-1 (HSV-1) in the cornea. The subsequent corneal inflammation and neovascularization may lead to scarring and visual loss. The cellular and molecular mechanisms underlying HSK remain unknown. The presence of stromal HSV-1 viral proteins or antigens in the HSK cornea remains a subject of debate. It was recen...

2013
Elif Erdem Emine Kocabas Hande Taylan Sekeroglu Özlem Özgür Meltem Yagmur T. Reha Ersoz

A 7-year-old girl had presented with high body temperature and joint pain which continued for 3 days. Because of the prolonged history of unexplained fever, rash, bilateral nonpurulent conjunctival injection, oropharyngeal erythema, strawberry tongue, and extreme of age, incomplete Kawasaki disease was considered and started on an intravenous immunoglobulin infusion. Six days after this treatme...

Journal: :The British journal of ophthalmology 1991
I W Hurley A M Brooks D P Reinehr G B Grant W E Gillies

A series of 22 patients with crystals in the anterior segment of the eye was examined by specular microscopy. Of 10 patients with hypermature cataract and hyperrefringent bodies in the anterior chamber cholesterol crystals were identified in four patients and in six of the 10 in whom aspirate was obtained cholesterol crystals were demonstrated in three, two of these having shown crystals on spe...

2011
Akihiro Katayama Jun Wada Hitomi Usui Kataoka Hiroko Yamasaki Sanae Teshigawara Takahiro Terami Kentaro Inoue Motoko Kanzaki Kazutoshi Murakami Atsuko Nakatsuka Hitoshi Sugiyama Norio Koide Hideaki Bujo Hirofumi Makino

Familial lecithin:cholesterol acyltransferase deficiency (FLD) is an autosomal recessive disorder characterized by corneal opacity, hemolytic anemia, low high-density lipoprotein cholesterol (HDL-C) and proteinuria. Two novel lecithin:cholesterol acyltransferase (LCAT) mutations[c.278 C>T (p.Pro69Leu); c.950 T>C (p.Met293Thr)] were identified in a 27-year-old man and in a 30-year-old woman, res...

Journal: :The British journal of ophthalmology 1978
G J Johnson M Overall

Nine specimens of the corneas of patients from Labrador and Northern Newfoundland affected by spheroidal degeneration (climatic droplet keratopathy) have been examined microscopically. Histochemical stains confirmed studies of similar corneal degenerations from other geographical areas that the droplets contain a protein which does not have all the characteristic properties of elastic tissue. S...

2016
Gloria López-Valverde Elena Garcia-Martin José Manuel Larrosa-Povés Vicente Polo-Llorens Luis E. Pablo-Júlvez

PURPOSE The purpose of this study is to describe a case of ocular rosacea with a very complex evolution. Rosacea is a chronic dermatological disease that may affect the ocular structures up to 6-72% of all cases. This form is often misdiagnosed, which may lead to long inflammatory processes with important visual consequences for affected patients. Therefore, an early diagnosis and an adequate t...

Journal: :Acta clinica Croatica 2012
Jasna Pavicić-Astalos Valentina Lacmanović-Loncar Ivanka Petric-Vicković Dean Sarić Zdravko Mandić Tigrena Csik Nikola Susić

The aim is to present a patient with severe bilateral corneal complications after long-term antiglaucoma treatment with 1% pilocarpine hydrochloride (Pilokarpin, Pliva, Zagreb, Croatia) and its management. A patient with narrow-angle glaucoma treated with 1% topical pilocarpine hydrochloride eye drops for the last twenty years complained of impaired vision, intermittent visual haloes and eye re...

Journal: :The British journal of ophthalmology 2003
M F El-Ashry M M Abd El-Aziz D F P Larkin B Clarke I A Cree A J Hardcastle S S Bhattacharya N D Ebenezer

AIMS To establish a clinical, histopathological, and genetic diagnosis in two unrelated British families with Avellino corneal dystrophy (ACD). METHODS Genomic DNA was extracted from peripheral blood leucocytes of all members participating in the study. Exons 4 and 12 of the human transforming growth factor beta induced (BIGH3) gene were amplified by polymerase chain reaction. The mutation an...

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