نتایج جستجو برای: behcets syndrome diagnosis

تعداد نتایج: 1029070  

Journal: :Arthritis & Rheumatism 1985

Journal: :Kidney International 2004

Ahmad Salimzadeh Ahmadreza Rajaee Fatemeh Moeineddin Hayedeh Ghaninejad Masoud Asgari

Recently multiple cutaneous leiomyomas, uterine leiomyoimatosis and renal cancer have been described as a cancer syndrome with autosomal dominant pattern of inheritance.We report a 79-year-old man who presented with multiple hyperkertotic erythematous nodules on his right leg with histological diagnosis of pilar leiomyoma. In his past medical history several systemic co...

Journal: :SAS Journal of Medicine 2020

Ezzat Dadkhah, Masood Ziaee Mohammad Hossein Davari Mohammad Reza Abbaszadegan, Toba Kazemi,

Objective(s)Marfan syndrome (MFS) is a severe connective tissue disorder withan autosomal dominant inheritance pattern. Early diagnosis is critical in MFS. Because of the large size of fibrillin-1 gene (FBN1), the uniqueness of mutations, and the absence of genotype-to-phenotype correlations linkage analysis can be very helpful for early diagnosis of MFS. In this study, eight polymorphic marker...

ژورنال: دانشور پزشکی 2011

Background and Objective: Carpal tunnel syndrome (CTS) is the most common entrapment neuropathy with involvement of median nerve. Patients with this syndrome refer for pain and paresthesia in hand that leads to thenar muscles atrophy. Diagnosis of CTS is made by history, physical examination and electrophysiological study. Recently, Volar Hot Dog (VHD) sign has been proposed for diagnosis of th...

Journal: :Revista Brasileira de Medicina do Esporte 2018

Journal: :The Kurume Medical Journal 1976

Journal: :Pan African Medical Journal 2021

Journal: :iranian journal of basic medical sciences 0
ezzat dadkhah department of human genetics, immunology research centre, avicenna research institute, mashhad university of medical science, mashhad, iran masood ziaee birjand hepatitis research centre, birjand university of medical sciences, birjand, iran mohammad hossein davari ophthalmology department, vali-e-asr hospital, birjand university of medical sciences, iran toba kazemi birjand atherosclerosis and coronary artery research centre, birjand university of medical sciences, birjand, iran mohammad reza abbaszadegan department of human genetics, immunology research centre, avicenna research institute, mashhad university of medical science, mashhad, iran medical genetic research centre (mgrc), school of medicine, mashhad university of medical sciences, mashhad, iran

objective(s)marfan syndrome (mfs) is a severe connective tissue disorder withan autosomal dominant inheritance pattern. early diagnosis is critical in mfs. because of the large size of fibrillin-1 gene (fbn1), the uniqueness of mutations, and the absence of genotype-to-phenotype correlations linkage analysis can be very helpful for early diagnosis of mfs. in this study, eight polymorphic marker...

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