نتایج جستجو برای: goldenhars syndrome

تعداد نتایج: 621911  

Journal: :acta medica iranica 0
alireza namazi shabestari department of gerontology, school of medicine, tehran university of medical sciences, tehran, iran. mojgan asadi osteoporosis research center, endocrinology and metabolism clinical sciences institute, tehran university of medical sciences, tehran, iran. and endocrinology and metabolism research center, endocrinology and metabolism clinical sciences institute, tehran university of medical sciences, tehran, iran. zahra jouyandeh obesity and eating habit research center, endocrinology and metabolism institute, tehran university of medical sciences, tehran, iran. mostafa qorbani department of medicine, school of medicine, karaj university of medical sciences, alborz, iran. and department of epidemiology, school of medicine, iran university of medical sciences, tehran, iran. roya kelishadi department of pediatrics, child growth and development research center, isfahan university of medical sciences, isfahan, iran.

the lipid accumulation product is a novel, safe and inexpensive index of central lipid over accumulation based on waist circumference and fasting concentration of circulating triglycerides. this study was designed to investigate the ability of lipid accumulation product to predict cardio-metabolic risk factors in postmenopausal women. in this cross-sectional study, 264 postmenopausal women by u...

Journal: :archives of trauma research 0
naseemul gani department of orthopedics, govt hospital for bone and joint surgery barzullah, srinager, india hayat ahmad khan department of orthopedics, govt hospital for bone and joint surgery barzullah, srinager, india; department of orthopedics, govt hospital for bone and joint surgery barzullah, srinager, india. tell: +91-9906672626, fax: +91-194-2423389 younis kamal department of orthopedics, govt hospital for bone and joint surgery barzullah, srinager, india munir farooq department of orthopedics, govt hospital for bone and joint surgery barzullah, srinager, india hina jeelani department of orthopedics, govt hospital for bone and joint surgery barzullah, srinager, india adil bashir shah department of orthopedics, govt hospital for bone and joint surgery barzullah, srinager, india

conclusion the anterior tarsal tunnel syndrome is a known disease. a high index of clinical suspicion is required while dealing with the chronic cases. a detailed history to rule out any traumatic event is necessary too. timely investigations and surgical release give dramatic relief. case presentation a 40 -year-old male patient was presented with the history of persistent pain along the dorsa...

Journal: :iranian journal of public health 0
m sahebjamee dept. of oral medicine, faculty of dentistry, tehran university of medical sciences, iran ng ameri dept. of oral medicine, faculty of dentistry, tehran university of medical sciences, iran dd farhud genetic clinic, vallie asr sq., 16 keshavarz blvd, tehran, iran.

noonan syndrome is an autosomal dominant disorder that is typically evident at birth. in many affected individuals, this syn­drome is associated with cardiac defects and a distinctive facial appearance. the high frequency of cardiac disorder, oph­thalmic, growth and orthopedic signs, associated with noonan syndrome emphasizes the need for early diagnosis. this re­port aimed to present a 19 year...

Abhimanyu Bhattacharya, Aditya Kanoi, Ashwin Alke Pai, Madhumita Gupta, Raghavendra Sawarappa, Ravi Ramachandra, Subhakanta Mohapatra,

Apert syndrome is a congenital craniosynostosis syndrome comprising of bilateral coronal synostosis , symmetric syndactyly of hands and feet and midface hypoplasia. We present an atypical phenotype of this syndrome with right sided unilateral coronal synostosis. However, type I apert hand and other clinical and radiological features suggestthe diagnosis. Genetic analysis revealed an absence of ...

امینی, علی,

Ballantyne syndrome is a syndrome with severe hydropic placenta and fetus followed by maternal hydrops. Several different causes may lead to this syndrome. In fact, Ballantyne syndrome may result from any factor causing severe hydrops fetalis. The diagnosis can be supported by sudden and rapid weight gain, severe edema, oliguria with albuminuria, blood pressure less than 140 mmHg and hemo...

Sasan Fallahi, Elham Ahmadi, Masoomeh Hasani Tabatabaei, Mojgan Alaeddini,

Background: Sj?gren’s syndrome is an autoimmune syndrome involving the exocrine glands specially the salivary and lacrimal glands leading to xerostomia and xerophtalmia. This paper presents a case with primary Sj?gren’s syndrome that severe dental caries were the first clinical manifestation. Case Presentation: A 42-year-old man was referred to the School of Dentistry, Tehran University of Medi...

Journal: :iranian journal of child neurology 0
parvaneh karimzadeh 1. professor of pediatric neurology, pediatric neurology research center, shahid beheshti university of medical sciences (sbmu), tehran, iran 2. professor of pediatric neurology, pediatric neurology department, mofid children hospital, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran mohammadkazem bakhshandeh bali 3. fellow of pediatric neurology, pediatric research center, shahid beheshti university of medical sciences (sbmu), tehran, iran mohammad mahdi nasehi assistant professor of pediatrics, department of pediatrics, mazandaran university of medical sciences, sari, iran seyedeh mohaddese taheri otaghsara general physician, tehran university of medical sciences, tehran, iran mohammad ghofrani 1. professor of pediatric neurology, pediatric research center, shahid beheshti university of medical sciences (sbmu), tehran, iran 2. professor of pediatric neurology, pediatric neurology department, mofid children hospital, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran

how to cite this article: karimzadeh p, bakhshandeh bali mk, nasehi mm, taheri otaghsara sm, ghofrani m. atypical findings of guillain-barré syndrome in children. iran j child neurol autumn 2012;6(4):17-22.   abstract objective guillain-barre syndrome (gbs) is an immune-mediated polyneuropathy that occurs mostly after  prior infection. the diagnosis of this syndrome is dependent heavily on the ...

Journal: :journal of research in medical sciences 0
mojgan sanjari assistant professor, kerman physiology research center, kerman university of medical sciences, kerman, iran mandana khodashahi resident, department of internal medicine, school of medicine, kerman university of medical sciences, kerman, iran ahmad gholamhoseinian professor, department of biochemistry, school of medicine, kerman university of medical sciences, kerman, iran mostafa shokoohi epidemiologist, research center for modeling in health (rcmh), kerman university of medical sciences, kerman, iran

normal 0 false false false en-us x-none fa background : an inverse association between serum adiponectin level and metabolic syndrome was seen in few studies. the aim of this study was to assess the association between serum adiponectin levels and metabolic syndrome in a sample of iranian women from kerman. methods : in a cross-sectional study 946 subjects were studied to determine the prevalen...

Journal: :iranian journal of child neurology 0
b.sh. shamsian md assistant professor, department of pediatric hematology-oncology,mofid children's hospital,shaid beheshti medical university m.t. arzanian md assistant professor ,cheif of hematology-oncology ward, department of pediatric hematology-oncology, shaid beheshti medical university s. alavi md assistant professor, department of pediatric hematology-oncology, namazi hospital, shiraz university of medical sciences s. zareifar md assistant professor, department of pediatric hematology-oncology, namazi hospital, shiraz university of medical sciences

abstract: griscelli syndrome (gs) is a rare disease first described in 1978. it is inherited in autosomal recessive pattern. this disease is characterized by partial albinism, pigmentation dilution, cellular immunodeficiency, neurological involvement & uncontrolled phases of macrophage & lymphocyte activation. we report a 5 months old iranian girl presenting with silver-gray hair,eyelashes and ...

Journal: :iranian journal of otorhinolaryngology 0
shahin abdollahi fakhim department of otorhinolaryngology, tabriz university of medical sciences, tabriz, iran nikzad shahidi department of otorhinolaryngology, tabriz university of medical sciences, tabriz, iran mehrnoush mousaviagdas department of otorhinolaryngology, tabriz university of medical sciences, tabriz, iran

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 inheritan...

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