PW01-037 – Amyloidosis probability depending on MEFV type

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منابع مشابه

PW01-037 – Amyloidosis probability depending on MEFV type

Methods 69 FMF patients (37 with amyloidosis, 32 – without amyloidosis) were investigated. All 69 patient underwent molecular-genetic investigation (PCR method), 9 different mutant combinations of MEFV gene were detected: 3 homozygous M694V/M694V(AA) in 25 patients, M680I/ M680I(CC) in 4, V726A/V726A(BB) in 1, 5 compound heterozygous M694V/V726A(AB) in 17, M694V/M680I (AC) in 9, V726A/M680I(BC)...

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PW01-003 – Frequency of MEFV mutations in Turkish population

Introduction Data on the epidemiology of familial Mediterranean fever (FMF) and the prevalence of disease causing mutations among different ethnic groups and geographical regions around the world are insufficient. The prevalence of mutations that account for FMF in Turkey has been defined in the past by determining the frequency of MEFV mutations in affected individuals or in hospital-based con...

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PW01-014 – MEFV methylation analysis in FMF and JRA diseases

Introduction MEFV is the first identified autoinflammatory gene related to Familial Mediterranean Fever (FMF) disease. We previously the tested the hypothesize of epigenetic involvement in FMF, mainly based on the occurrence of FMF in patients without mutations and decreased MEFV transcripts in leukocyte samples independent from mutations. Our study showed that higher methylation level of MEFV ...

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PW01-020 – MEFV mutations carrier rate in Central Europe

Introduction Familial Mediterranean fever (FMF) is an autosomalrecessive disorder characterized by recurrent attacks of fever and serositis common in eastern Mediterranean population. Over 160 mutations have been identified in MEFV gene responsible for FMF. The most common mutations in MEFV gene are E148Q, M694I, M694V, V726A and M680I. The distribution pattern of MEFV mutation along the Medite...

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PW01-019 – MEFV gene mutations in 53 periodic fever patients

Methods We collected clinical and laboratory data from periodic fever patients followed at our center from the beginning of 2006 to the end of 2012. Results of genetic testing for MEFV gene mutations were also collected. Genetic testing was performed in Genetic laboratory of University Children’s Hospital Ljubljana. All 10 exons and exon/ intron regions of MEFV gene were directly sequenced with...

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ژورنال

عنوان ژورنال: Pediatric Rheumatology

سال: 2013

ISSN: 1546-0096

DOI: 10.1186/1546-0096-11-s1-a90