نتایج جستجو برای: mefv mutation

تعداد نتایج: 292011  

2015
Noriyoshi Ishikawa Chika Amano Takeshi Taketani Koji Kumori Yuji Harada Hisayuki Hiraiwa Kayoko Itamura Riruke Maruyama

Nephrogenic adenoma, also referred to nephrogenic metaplasia, is a benign proliferative lesion of urothelium, usually associated with chronic physical stimuli or inflammation. Familial Mediterranean fever is an inherited autosomal recessive disease characterized by recurrent short episodes of fever. The site of mutation is found in MEFV gene which controls inflammatory responses. We have experi...

Journal: :cell journal 0

objective: familial mediterranean fever (fmf) is an autosomal recessive disorder characterized by recurrent febrile attacks accompanied by serosal and synovial membrane inflammation. fmf is caused by mutations in the mefv gene and are found usually among mediterranean populations, armenians, turks, arabs and jews. the aim of this study was to determine the frequency of mefv gene mutations among...

Journal: :Clinical genetics 2013
C Zizzo P Colomba G Albeggiani R Gallizzi F Iemolo D Nuzzo S Vasto C Caruso G Duro

Fabry disease (FD) is an underdiagnosed pathology due to its symptomatology that overlaps with various systemic and rheumatic disorders, including familial Mediterranean fever (FMF). We examined the Mediterranean fever (MEFV) and α-galactosidase A (GLA) genes, whose mutations are responsible for FMF and FD, respectively, in 42 unrelated patients diagnosed with FMF, which revealed significant am...

Journal: :European journal of rheumatology 2016
Sabri Güncan N Şule Y Bilge Döndü Üsküdar Cansu Timuçin Kaşifoğlu Cengiz Korkmaz

OBJECTIVE This study aimed to investigate the frequency in which familial Mediterranean fever (FMF) coexists with other diseases and determine whether Mediterranean fever (MEFV) gene mutations are involved in such coexistence. MATERIAL AND METHODS In total, 142 consecutive patients with FMF investigated for MEFV mutation were enrolled in this study [Female: 87; Male: 55, mean age 32±12 years ...

Journal: :Annals of human genetics 2008
V P Papadopoulos S Giaglis I Mitroulis K Ritis

Our aim was to construct a Familial Mediterranean Fever (FMF) cumulative database and to propose a MEFV based phylogenetic tree. Data were collected from published studies. A meta-analysis based on 16,756 chromosomes from FMF patients and normal individuals from 14 affected populations was performed. Arlequin 2.0 and Phylip 3.2 software were used for population genetics analysis and phylogeneti...

Journal: :Turkish journal of medical sciences 2014
Hülya Sümer Çelebı Hilal Özdağ

BACKGROUND/AIM Sensitive and cost-effective detection of point mutations is important in genetics research. Denaturing high-performance liquid chromatography (DHPLC) is known to be one of the most sensitive techniques for point mutation detection. A more recent technique, high-resolution melting (HRM), is based on the melting behavior of PCR products. In this study, the efficiency and sensitivi...

Journal: :Clinical and experimental rheumatology 2008
K Migita T Nakamura Y Maeda T Miyashita T Koga M Tanaka M Nakamura A Komori H Ishibashi T Origuchi H Ida E Kawasaki M Yasunami K Eguchi

OBJECTIVE Familiar Mediterranean Fever (FMF) is common among Mediterranean populations, while other populations are rarely affected. The aim of this study was to assess the involvement of MEFV gene mutations among Japanese rheumatoid arthritis patients with or without amyloid A (AA) amyloidosis. METHODS The frequency of the MEFV mutations, which were identified in Japanese FMF patients, was d...

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...

2014
Dai Kishida Akinori Nakamura Masahide Yazaki Ayako Tsuchiya-Suzuki Masayuki Matsuda Shu-ichi Ikeda

INTRODUCTION Familial Mediterranean fever (FMF) is a hereditary autoinflammatory disease characterized by recurrent self-limiting fever and serositis that mainly affects Mediterranean populations. Many patients with FMF have been reported in Japan due to increasing recognition of this condition and the availability of genetic analysis for the gene responsible, MEFV. The present study was perfor...

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