Familial Mediterranean fever is inherited in an autosomal recessive manner. There are two
phenotypes: types 1 and 2. Familial Mediterranean fever type 1 is characterized by recurrent …

Secondary amyloidosis is the most severe complication of familial Mediterranean fever
(FMF). Since the M694V mutation was associated with clinical severity, it was expected to be …

The aim of this study was to determine the relationship between clinical findings and the
most common mutated alleles of MEFV gene in a childhood population and to determine the …

Abstract Familial Mediterranean Fever (FMF) which is frequently present in Mediterranean
populations is caused by mutations in the MEFV gene. According to recent data, MEFV …

Familial Mediterranean fever (FMF) is divided into two phenotypes: type 1 and type 2. FMF
type 1 is characterized by recurrent short episodes of inflammation and serositis including …

Abstract Familial Mediterranean Fever (FMF) is an autoinflammatory periodic disorder. We
aim to identify the distribution and the frequency of the Mediterranean Fever (MEFV) gene …

In the present study, 1000 patients with clinical suspicion of FMF were retrospectively
reviewed to determine the spectrum of MEFV gene mutations by using DNA sequence …

Objective. Our knowledge about the frequencies of mutations in the Turkish population is
based on the studies on the affected patients and hospitalbased control groups. We aimed …

In this study we have retrospectively analysed the mutation spectrum of the 351 Familial
Mediterranean fever patients referred to Kırıkkale University Faculty of Medicine, Department …

Familial Mediterranean fever (FMF) is an autosomal recessive hereditary disease commonly
observed around the Mediterranean basin presenting as recurrent febrile episodes. We …