نتایج جستجو برای: ocular disorder

تعداد نتایج: 645586  

2014
Krati Chauhan Clement Michet

We present a case of systemic granulomatous disorder/Blau syndrome. A patient was seen at our clinic with a diagnosis of Juvenile Idiopathic Arthritis (JIA). He was diagnosed with polyarticular JIA when he was two years old, at that time primary manifestations included inflammation of the hand and wrist joints bilaterally, later he developed ocular symptoms, which were attributed to JIA. He had...

2007
Benedikt GH Schoser

Ocular myositis represents a subgroup within the idiopathic orbital inflammatory syndrome, formerly termed orbital pseudotumor. Ocular myositis describes a rare inflammatory disorder of single or multiple extraocular eye muscles. Unilateral or sequential bilateral subacute painful diplopia is the leading symptom of eye muscle myositis. There are at least two major forms, a limited oligosymptoma...

2018
Jennifer C Hocking Jakub K Famulski Kevin H Yoon Sonya A Widen Cassidy S Bernstein Sophie Koch Omri Weiss Seema Agarwala Adi Inbal Ordan J Lehmann Andrew J Waskiewicz

The eye primordium arises as a lateral outgrowth of the forebrain, with a transient fissure on the inferior side of the optic cup providing an entry point for developing blood vessels. Incomplete closure of the inferior ocular fissure results in coloboma, a disease characterized by gaps in the inferior eye and recognized as a significant cause of pediatric blindness. Here, we identify eight pat...

Journal: :Vision Research 1993
M. Monteico-Guillo A. P. Souse J. Galvao M. Yuch C. Marques-Neves J. Riberto-da-Silva

In Portugal, the prevalence of human immunodeficiency virus type 2 (HIV-2) seropositivity is higher than in other European countries or North America. Recent literature data points out a possible difference on the pathogenic potential and on the natural history of HIV-1 and HIV-2, suggesting a lower virulence of HIV-2. Facing these hypothesis and the increasing number of HIV-2 cases, we analyse...

Bahareh Kardideh, Fatemeh Khademi, Hamid-Reza Mohammadi-Motlagh, Kamran Mansouri, Mehran Pournazari, Parviz Soufivand, Shirin Assar,

Background: Rheumatoid Arthritis patients are evaluated during treatment for various inflammatory factors such as C-reactive protein, Erythrocyte Sedimentation Rate, and Disease Activity Score, and other immune system-related factors. In the follow-up of patients with rheumatoid arthritis, hematologic factors associated with the immune system especially Platelet to Lymphocyte Ratio and Neutroph...

Afshin Raufi Alireza Bahonar, Majid Masudi fard Seyed Hossein Moadab Taghi Bazargani,

The aim of this study was to determine the prevalence and type of ophthalmic diseases among horse populations in the suburbian riding clubs of Tehran. Ophthalmologic examinations were performed in 901 horses and ocular lesions were diagnosed in 40 (4.4%) animals. In the 54 eyes of these horses that had ocular defects, 103 ocular abnormalities were detected. Of those horses affected, 65% showed ...

hazavehei, mohammad mehdi, kashfi, mansour, khani jeihooni, ali,

Background & Objective: With respect to increasing prevalence of diabetes, the chance for incidence of ocular complications among diabetics, this study was conducted to investigate the prevalence and risk factors for the incidence of the ocular complications in the patients referred to the Nader Kazemi Shiraz Diabetic center from 1998 to 2010.Materials & Methods: In a cross sectional study , su...

2016
Suman Verma Kavita Paul Narendra Kumar Bairwa

Corresponding authorDr. Kavita Paul,Department of Medicine,GGS Medical College and Hospital,Faridkot, 151203, Punjab, India.Email: [email protected] This article may be cited as:Paul K,Kazal HL,Bairwa NK,Verma s. Marfan syndrome a rare genetic disorder: A case report 2016;2(1):33-6 Article Recieved On: 10-2-16 Accepted On: 19-3-2016 NTRODUCTION Marfan syndrome (MFS) is a spectrum disorder ...

Journal: :AJNR. American journal of neuroradiology 1999
C Parazzini F Triulzi G Russo M Mastrangelo G Scotti

Encephalocraniocutaneous lipomatosis (ECCL) is a rare neurocutaneous syndrome characterized by unilateral scalp, facial, and ocular lesions and ipsilateral cerebral malformations. To define the neuroimaging features of this disorder we studied two patients affected by ECCL and compared our data with those reported in the literature. Sonographic, CT, and MR imaging examinations showed quite spec...

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