نتایج جستجو برای: weils syndrome

تعداد نتایج: 621915  

Journal: :iranian journal of child neurology 0
ali akabar asadi-pooya 1.neurosciences research center, shiraz university of medical sciences, shiraz, iran 2.jefferson comprehensive epilepsy center, department of neurology, thomas jefferson university, philadelphia, usa mohaddese sharifzade neurosciences research center, shiraz university of medical sciences, shiraz, iran

how to cite this article: asadi-pooya aa, sharifzade m. west syndrome in south iran: electro-clinical manifestations. iran j child neurol. 2013 summer; 7(3): 40-44. objective we aimed to determine the clinical and electroencephalographic (eeg) characteristics of the patients with west syndrome (ws) in south iran. materials & methods in this retrospective study, all patients with a clinical diag...

Journal: :گوارش 0
ahmad khodadad mehri najafi-sani fatemeh famouri v modaresi

allgrove syndrome also known as triple-a syndrome is an autosomal recessive disorder characterized by alacremia, achalasia and acth-resistant adrenal insufficiency. although this syndrome is rare, herein we report four cases with different clinical manifestations. they were referred to the gastrointestinal ward during a one year period with complaints of vomiting and dysphagia. the diagnosis of...

Journal: :نشریه پرستاری ایران 0
فریبا نصیری زیبا fariba nasiri-ziba

carpal tunnel syndrome is known as an industrial new epidemic. in many of jobs, the same motions of hand are repeated thousands of times a day.  each day the number of people with the syndrome is increasing. clerks, workers in food preparation and packaging, and secretaries of large supermarkets have a high risk for suffering from this syndrome. in fact, all people who flex and extend their wri...

Journal: :iranian red crescent medical journal 0
jun-li tsai md, department of family medicine, cheng ching general hospital, taichung, taiwan shang-feng tsai md, division of nephrology, department of internal medicine, taichung veterans general hospital, taichung, taiwan; school of medicine, china medical university, taichung, taiwan; department of life science, tunghai university, taichung, taiwan; md, division of nephrology, department of medicine, taichung veterans general hospital, taichung, taiwan. tel: +886-423592525, fax: +886-423594980

introduction urinary tract infection is a common disease in the general population. however, in patients with frequent urinary tract infection, it is important to determine any treatable cause to avoid recurrence. case presentation herlyn-werner-wunderlich syndrome or ohvira syndrome is a very rare congenital anomaly with uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis. ...

Journal: :iranian rehabilitation journal 0
sahel hemmati social welfare and rehabikitation university , kodakyar blv, evin, tehran farin soleimani kodakyar blv, evin, tehran reza seyednour social welfare & rehabilitation university , kodakyar blv, evin, tehran asghar dadkhah iranian research center on aging, university of social welfare and rehabilitation sciences, teran, iran.

objectives: stigma is a negative value. many behaviors are to ward stigmatized people. down syndrome is one of conditions with stigma. the aim of this study is to determine the sources of labeling in iranian down syndrome. methods: the view of 105 down syndrome families concerning stigma were conducted. all of down syndrome was under 50 years. results: a fair proportion of down syndrome familie...

Thromboembolism is a rare complication of primary nephortic syndrome. Both venous and arterial thrombosis might occur in steroid responsive and steroid resistant nephrotic syndrome. This is the report of an infant with nephrotic syndrome and renovascular hypertension, complicated with asymptomatic intracardiac thrombus and managed appropriately with medical treatment.

Ali Akbar Akaberi, Fariba Binesh Saeed Amini

Unilateral nevoid telangiectasia syndrome (UNTS) can be classified into two major categories: congenital and acquired. There have been reports showing an increase in skin estrogen and progesterone receptors in patients with this syndrome. We report a male patient with acquired unilateral nevoid telangiectasia syndrome without any associated physiological or pathological conditions.<...

Apert syndrome is a genetic defect which was first described by Eugene Apert in 1906. itchr('39')s incidence is approximately one in 50000 births. This syndrome is many abnormalities in your body and Central Nervous System. rehabilitation can increase children and their parentchr('39')s quality of life.We report a case of Apert syndrome and his occupational therapy program.

Mehrnoush Mousaviagdas Nikzad Shahidi, Shahin Abdollahi Fakhim

Introduction: Nager syndrome is a malformation resulting from problems in the development of the first and second branchial arches and limb buds. The cause of the abnormal development of the pharyngeal arches in Nager syndrome is unknown. It is also unclear why affected individuals have bone abnormalities in their arms and legs. Nager syndrome is thought to have an autosomal recessive inherita...

حبیبی, منیژه, خشک رود منصوری, بابک, زالی , محمدرضا , صفائی, آزاده, مقیمی دهکردی , بیژن , پورحسینقلی , اسما , پورحسینقلی , محمد امین ,

  Abstract   Background & Aims : Irritable bowel syndrome is a common functional gastro-intestinal disease. Patients can experience symptoms for many years. These symptoms have significant impact on patient’s quality of life. There is a little information about irritable bowel syndrome in Iran. The aim of the present study was to determine the prevalence of irritable bowel syndrome by using the...

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