نتایج جستجو برای: ocular abnormalities

تعداد نتایج: 156050  

Journal: :American family physician 2013
Amanda L Bell Mary Elizabeth Rodes Lisa Collier Kellar

Vision screening in children is an ongoing process, with components that should occur at each well-child visit. The purpose is to detect risk factors and visual abnormalities that necessitate treatment and to identify those patients who require referral to an ophthalmologist skilled in examining children. Screening can reveal conditions commonly treated in primary care and can aid in discussion...

2014
Andrea Sodi Sara Matteoli Giovanni Giacomelli Lucia Finocchio Andrea Corvi Ugo Menchini

Background. The aim of this study is to investigate the ocular thermographic profiles in age-related macular degeneration (AMD) eyes and age-matched controls to detect possible hemodynamic abnormalities, which could be involved in the pathogenesis of the disease. Methods. 32 eyes with early AMD, 37 eyes with atrophic AMD, 30 eyes affected by untreated neovascular AMD, and 43 eyes with fibrotic ...

2017
Zixi Sun Qi Zhou Huajin Li Lizhu Yang Shijing Wu Ruifang Sui

Purpose This study aims to describe the phenotypes and identify pathogenic mutations in Chinese patients who have congenital cataracts associated with other ocular abnormalities. Methods Eleven patients from four unrelated Chinese families plus two simplex cases were enrolled in this study. Detailed ophthalmic examinations were performed. DNA samples were isolated from peripheral blood collec...

Journal: :The British journal of ophthalmology 2000
M M van Genderen G F Kinds F C Riemslag R C Hennekam

AIMS To delineate the nature and frequency of ocular pathology in Rubinstein-Taybi syndrome (RTs). METHODS Literature was searched for reports describing ocular symptoms in patients with RTs. 24 RTs patients (out of a total of 73 Dutch known RTs individuals) were selected for ophthalmological and electrophysiological examination, selection being based only on the distance between a patient's ...

Journal: :AJNR. American journal of neuroradiology 1997
M A Sargent K J Poskitt J E Jan

PURPOSE To determine the frequency of cerebellar and cerebral abnormalities on brain imaging studies in children with congenital ocular motor apraxia. METHODS Brain imaging studies were performed in 19 children with typical congenital ocular motor apraxia who were in the care of a visual impairment program at a children's hospital. Independent clinical review categorized the subjects as havin...

Mohammadsaeed Ahrarikhafi, Saghar Karimi Sina Salavati

Objective- The aim of this study was to evaluate ultrasonographic appearance of the normal eye and obtaining reference values of ocular structures in Iranian native donkey. Design- Experimental study. Animals- Five Iranian native donkeys. Procedures- After preparation of the animals, ocular structures were ima...

Journal: :Acta ophthalmologica Scandinavica 2001
S Grönqvist O Flodmark K Tornqvist G Edlund A Hellström

PURPOSE To characterise the nature and degree of ocular disorders and cerebral morphological and functional abnormalities in a population-based group of visually impaired full-term pre-school children. METHODS Forty-five children who were born at full-term between 1989 and 1995 in Värmland, Sweden, were reported as being visually impaired. An ophthalmological examination was performed and cli...

Journal: :Annals of optometry and contact lens 2022

Dry eye disease (DED) is a condition of the ocular surface characterized by tear film abnormalities and symptoms; inflammation principal pathogenesis. Recently, matrix metalloproteinase-9 (MMP-9) point-of-care immunoassay (InflammaDry) has become widely used as an ancillary diagnostic tool in routine clinical settings. This paper reviews role MMP-9 DED, relationships MMP-9-positivity on Inflamm...

Journal: :Journal of medical genetics 1998
H E Cunliffe L A McNoe T A Ward K Devriendt H G Brunner M R Eccles

The PAX2 gene is mutated in patients with ocular colobomas, vesicoureteral reflux (VUR), and kidney anomalies (renal-coloboma syndrome, OMIM 120330). The three abnormalities which make up this syndrome also occur in isolation, but the causal genes are not known. PAX2 encodes a transcription factor of the paired box class of DNA binding proteins, important for the development of the urogenital t...

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