Autoinflammatory diseases (AIDs) represent a rare and heterogeneous group of disorders
characterized by recurrent episodes of inflammation and a broad range of clinical …

Familial Mediterranean fever (FMF) is a genetic autoinflammatory disease with autosomal
recessive transmission, characterized by periodic fever attacks with self-limited serositis …

Familial Mediterranean Fever (FMF) is a hereditary autoinflammatory disease characterized
by an early onset of recurrent fever and serositis episodes. FMF is caused by mutations in …

Recurrent abdominal pain is a common reason for repeated visits to outpatient clinics and
emergency departments, reflecting a substantial unmet need for timely and accurate …

Objectives FMF is the most common hereditary monogenic fever syndrome marked by
recurrent attacks of fever and polyserositis. Colchicine is the current recommended first-line …

Familial Mediterranean fever (FMF) is the most common monogenic autoinflammatory
disease and is usually diagnosed in childhood, especially in the first decade of life …

Objectives To develop a novel scoring system to predict colchicine resistance in Familial
Mediterranean fever (FMF) based on the initial features of the patients. Methods The medical …

Familial Mediterranean fever (FMF), the most frequent monogenic autoinflammatory
disease, is manifested with recurrent and chronic inflammation and amyloid A (AA) …

Objectives This study aimed to evaluate the clinical, laboratory and genetic characteristics
and outcomes of patients with AA amyloidosis. Methods Patients followed up in a tertiary …

Familial Mediterranean fever (FMF) is a periodic fever syndrome caused by variation in
MEFV. FMF is known for IL-1β dysregulation, but the innate immune landscape of this …