Behcet-like familial autoinflammatory syndrome
نویسندگان
چکیده
منابع مشابه
A heterozygous variant in MEFV in a familial autoinflammatory syndrome with PAPA-like features
Introduction Autoinflammatory disorders are a group of diseases whose nosology and etiology are only partly understood. Among Mendelian forms, familial Mediterranean fever (FMF), due to mutations in MEFV, is one of the most frequent. Most MEFV mutations are located in exon 10 and are usually associated with an autosomal recessive mode of inheritance. MEFV encodes pyrin, which interacts with PST...
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Introduction Human Autoinflammatory Diseases (HADs) is a heterogeneous group of rare genetic diseases, which are characterized by unprovoked onsets of inflammation, fever and clinical symptoms analogous with rheumatic diseases with absence of immunological indicators. Familial Mediterranean Diseases (FMF) is one of the popular forms in the group of syndromes which are called HPFS. Clinical char...
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73 Received December 20, 2013; revised and accepted April 23, 2014. Published online May 16, 2014; doi: 10.1620/tjem.233.73. Correspondence: Kiyoshi Migita, M.D., Clinical Research Center, NHO Nagasaki Medical Center, Kubara 2-1001-1, Omura, Nagasaki 856-8652, Japan. e-mail: [email protected] Overlap Syndrome between Familial Mediterranean Fever and Tumor Necrosis Factor Receptor-Associate...
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ژورنال
عنوان ژورنال: Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics)
سال: 2021
ISSN: 2500-2228,1027-4065
DOI: 10.21508/1027-4065-2021-66-2-110-115