Genetic Analysis of MEFV Gene Pyrin Domain in Patients With Behçet's Disease [PDF]
Objectives. Behçet's disease (BD) is a systemic vasculitis with recurrent oral and genital ulcers and uveitis. MEFV gene, which is the main factor in familial Mediterranean fever (FMF), is also reported to be a susceptibility gene for BD.
Ahmet Dursun +5 more
doaj +7 more sources
Genewise detection of variants in MEFV gene using nanopore sequencing. [PDF]
Familial Mediterranean Fever (FMF) is a genetic disorder with complex inheritance patterns and genotype-phenotype associations, and it is highly prevalent in Armenia. FMF typically follows an autosomal recessive inheritance pattern (OMIM: 249100), though it can occasionally display a rare dominant inheritance pattern with variable penetrance (OMIM ...
Ghukasyan L +14 more
europepmc +4 more sources
A novel single variant in the MEFV gene causing Mediterranean fever and Behçet’s disease: a case report [PDF]
Background Familial Mediterranean fever is an autoinflammatory disease of unknown etiology, characterized clinically by recurrent attacks of sudden-onset fever with arthralgia and/or thoracoabdominal pain and pathogenetically by autosomal recessive ...
Maria Zerkaoui +4 more
doaj +2 more sources
The association of MEFV gene mutations with the disease risk and severity of systemic juvenile idiopathic arthritis [PDF]
Background Systemic juvenile idiopathic arthritis (sJIA) has many clinical features overlapping with familial Mediterranean fever (FMF), which is caused by mutations in MEFV gene. And FMF patients were easily misdiagnosed as sJIA in China.
Linqing Zhong +10 more
doaj +2 more sources
Analysis of MEFV exon methylation and expression patterns in familial Mediterranean fever [PDF]
Background MEFV mutations and decreased expression level of the gene are related to FMF pathology. DNA methylation at CpG islands is a well-known mechanism for transcriptional silencing.
Ozdogan Huri +6 more
doaj +3 more sources
Associations of MEFV gene variants, IL-33, and sST2 with the risk of Henoch-Schönlein purpura in children [PDF]
Objective: Henoch-Schönlein purpura (HSP) is the most common systemic vasculitis in children. HSP is a multifactorial inflammatory disease, but its pathogenesis is still unclear.
Yang Ruan, Longlong Xie
doaj +2 more sources
The clinical significance of the Mediterranean fever gene MEFV variants in Castleman disease [PDF]
Background Idiopathic Multicentric Castleman Disease, Thrombocytopenia, Anasarca, Fever, Reticulin Fibrosis, Organomegaly (iMCD-TAFRO) is a rare cytokine storm syndrome with high mortality.
Yumo Du +18 more
doaj +2 more sources
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.
Farhad Salehzadeh +4 more
doaj +2 more sources
Immunogenic Potential of the Mediterranean Fever Gene in Patients with Coronavirus Disease: A Cross-Sectional Study [PDF]
Background: In December 2019, an outbreak of pneumonia caused by the novel coronavirus disease 2019 (COVID-19) became a pandemic and caused a global health crisis.
Farhad Salehzadeh +5 more
doaj +1 more source
Improvement of MEFV gene variants classification to aid treatment decision making in familial Mediterranean fever. [PDF]
Accetturo M +3 more
europepmc +2 more sources

