News Medical: VIB researchers develop new tool to diagnose Familial Mediterranean Fever Researchers at VIB and Ghent University have developed a tool to diagnose Familial Mediterranean Fever (FMF). Particularly common among Mediterranean populations, this genetic disease is characterized ... Familial Mediterranean fever (FMF) is a hereditary inflammatory disorder.

Understanding the Context

[3]: 149 FMF is an autoinflammatory disease caused by mutations in the Mediterranean fever (MEFV) gene, which encodes a 781–amino acid protein called pyrin. [4] Familial Mediterranean fever (FMF) is a genetic condition that causes episodes of fever and inflammation that come and go throughout your life. It’s named for the fact that it usually affects people from Mediterranean ethnicities. Familial Mediterranean fever is an inherited condition characterized by recurrent episodes of painful inflammation in the abdomen, chest, or joints.

Familial Mediterranean Fever

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Key Insights

These episodes are often accompanied by fever and sometimes a rash or headache. Familial Mediterranean fever is an inherited condition characterized by recurrent episodes of painful inflammation in the abdomen, chest, or joints. Explore symptoms, inheritance, genetics of this condition. Familial Mediterranean fever is a rare genetic disease that often first appears in childhood as recurring fevers. Find out who’s at higher risk for FMF, how to treat it, and how to prevent ...

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Final Thoughts

What is Familial Mediterranean Fever? FMF is considered a rare disease worldwide. However, it is very common in people of Sephardic (non-Ashkenazi) Jewish, Armenian, Arab and Turkish heritage. Among people with these backgrounds, about 1 in 200 has FMF. Information on familial Mediterranean fever in children: what it is, common symptoms, getting diagnosed, and treatment options. Familial Mediterranean Fever - Etiology, pathophysiology, symptoms, signs, diagnosis & prognosis from the MSD Manuals - Medical Professional Version.