Familial Mediterranean Fever (FMF) is a hereditary autoinflammatory disease characterized by recurrent fever and systemic inflammation, most prevalent in Eastern Mediterranean populations.Rare in regions like Romania, FMF presents diagnostic science can solar system planetary electronic projector w/ 3 viewing discs challenges and risks severe complications if untreated.We report a 7-year-old Romanian girl, from a non-classical ethnic background, with recurrent febrile episodes and elevated inflammatory markers.Genetic testing confirmed a homozygous MEFV c.2082G>A (p.
Met694Ile) variant.Colchicine therapy reduced oolution light up flare frequency and normalized inflammatory markers.FMF should be considered in atypical populations with recurrent inflammation.Genetic testing aids diagnosis in non-endemic regions, enabling early colchicine treatment to prevent complications.