نتایج جستجو برای: ژن mefv

تعداد نتایج: 16785  

Farhad Salehzadeh, Mehdi Jafari Asl Saeid Hosseini Asl Sepideh Jahangiri Shahram Habibzadeh,

Familial Mediterranean Fever (FMF) is a hereditary autoinflammatory disease with autosomal recessive inheritance pattern often seen around the Mediterranean Sea. It is characterized by recurrent episodes of fever and polyserositis and rash. Recently, MEFV gene analysis determines the definitive diagnosis of FMF. In this study, we analyzed 12 MEFV gene mutations in more than 200 FMF patients, pr...

2016
F Battal F Silan N Topaloğlu H Aylanç Ş Yıldırım F Köksal Binnetoğlu M Tekin N Kaymaz O Ozdemir

The aim of the current study was to determine the frequency of the Mediterranean fever (MEFV) gene pathogenic variants in 60 children diagnosed with familial Mediterranean fever (FMF) and to compare the phenotype-genotype correlation. Genomic DNA was isolated by the spin-column method from peripheral blood samples (collected in vacutainers containing EDTA) and buccal smears. The MEFV gene profi...

2015
K Warrier L Cliffe L McDermott S Rangaraj

Background/question Familial Mediterranean Fever (FMF) is a hereditary inflammatory disorder characterised by self-resolving attacks of fever and serositis common in populations from Mediterranean ancestry [1]. Mutations affecting MEFV gene is believed to be responsible for the disease phenotype[1]. The correlation between the genotype and phenotype is not very strong, indicating the presence o...

2015
A Berdeli G Mukhtarova A Oz S Musayev

Introduction Familial Mediterranean fever (FMF)(MIM 249100) is a hereditary autoinflammatory disorder characterized by episodes of inflammation in the absence of high-titer autoantibodies or antigen-specific T cells. The Mediterranean fever (MEFV) gene(OMIM 608107) located on chromosome 16p13.3, which encodes the 781-amino-acid protein pyrin, is the causative gene for this monogenic Mendelian d...

Journal: :Human molecular genetics 1998
A Bernot C da Silva J L Petit C Cruaud C Caloustian V Castet M Ahmed-Arab C Dross M Dupont D Cattan N Smaoui C Dodé C Pêcheux B Nédelec J Medaxian M Rozenbaum I Rosner M Delpech G Grateau J Demaille J Weissenbach I Touitou

Familial Mediterranean fever (FMF) is an autosomal recessive disorder characterized by recurring attacks of fever and serositis. It affects primarily North African Jews, Armenians, Turks and Arabs, in which a founder effect has been demonstrated. The marenostrin-pyrin-encoding gene has been proposed as a candidate gene for the disease ( MEFV ), on the basis of the identification of putative mut...

2015
Kohei Fujikura

Familial Mediterranean fever (FMF) is an inherited disorder characterized by recurrent episodes of fever accompanied by sterile peritonitis, arthritis, and pleuritis. Many mutations in the MEFV gene have been identified as causing FMF. However, accompanying epidemiological information remains quite scarce except in some Mediterranean countries, and the degree of penetrance has been a subject of...

Journal: :Chest 1985
R B Berry R D Fairshter

The effects of deep inspiration upon expiratory flow rates and response to inhaled metaproterenol were studied in normal and asthmatic subjects using partial (PEFV) and maximal (MEFV) expiratory flow volume curves. Routine pulmonary function tests and specific conductance were also measured. Prior to administration of metaproterenol, 18 of 24 normal subjects and 11 of 24 asthmatic subjects (p 0...

Journal: :Clinical genetics 2013
F S Ong H Vakil Y Xue J Z Kuo K H Shah R B Lee K E Bernstein D L Rimoin T Getzug K Das J L Deignan J I Rotter W W Grody

Familial Mediterranean fever (FMF), inherited in an autosomal recessive manner, is a systemic auto-inflammatory disorder characterized by recurrent attacks of fever with peritonitis, pleuritis, synovitis and erysipeloid rash. The marenostrin-encoding fever (MEFV) gene, located on chromosome 16p13.3, is the only gene in which mutations are currently known to cause FMF. To correlate specific geno...

2013
K Takabe Y Adachi H Saito T Yamashita Y Wakai K Saito Y Shinohara

Introduction Familial Mediterranean Fever (FMF) is considered a rare disease in Japan. Our institution began screening for MEFV gene mutations in patients with periodic fever in 2005. Among the 18 patients screened, we have identified 11 (56.5%) FMF patients with heterozygous M694I/E148Q mutations. Among the other 7 patients, no pathogenic mutations were detected by the direct sequencing of all...

Journal: :Clinical and experimental rheumatology 2008
N Tomiyama Y Higashiuesato T Oda E Baba M Harada M Azuma T Yamashita K Uehara A Miyazato K Hatta Y Ohya K Iseki Y Jinno S Takishita

BACKGROUND Familial Mediterranean fever (FMF) is an autosomal recessive disease characterized by recurrent attacks of fever with serosal inflammation. FMF gene (MEFV) mutations have been identified primarily in patients from Mediterranean populations. Although several clinical cases have been reported in Japan, there have been few reports to date on mutation analysis. We studied FMF patients an...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید