Indication
Familial Mediterranean fever
Familial Mediterranean fever is an inherited autoinflammatory disorder caused by pathogenic variants in the *MEFV* gene, which encodes the pyrin protein involved in innate immune regulation. Read more about Familial Mediterranean fever
28 drugs 27 manufacturers
Drugs that treat it
Common Familial Mediterranean fever therapies.
COLCHICINE
COLCHICINE
COLCHICINE
COLCHICINE
COLCHICINE
COLCHICINE
ILARIS (canakinumab/PF)
COLCHICINE
News & literature
Coming soonRelated codes
Coming soonRelated conditions & guidelines
Coming soonFamilial Mediterranean fever is an inherited autoinflammatory disorder caused by pathogenic variants in the *MEFV* gene, which encodes the pyrin protein involved in innate immune regulation.
It primarily affects individuals of Mediterranean and Middle Eastern ancestry, with symptom onset typically occurring in childhood or young adulthood.
The condition is characterized by recurrent, self-limiting episodes of fever accompanied by painful serositis involving the peritoneum, pleura, synovium, or skin.
Without proper disease control, persistent systemic inflammation can lead to the accumulation of serum amyloid A protein, causing secondary renal amyloidosis and progressive kidney failure.
- medlineplus.gov
Familial Mediterranean fever is an inherited autoinflammatory disorder caused by pathogenic variants in the *MEFV* gene, which encodes the pyrin protein involved in innate immune regulation The condition is characterized by recurrent, self-limiting episodes of fever accompanied by painful serositis involving the peritoneum, pleura, synovium, or skin
- sobi.com
Familial Mediterranean fever is an inherited autoinflammatory disorder caused by pathogenic variants in the *MEFV* gene, which encodes the pyrin protein involved in innate immune regulation It primarily affects individuals of Mediterranean and Middle Eastern ancestry, with symptom onset typically occurring in childhood or young adulthood Without proper disease control, persistent systemic inflammation can lead to the accumulation of serum amyloid A protein, causing secondary renal amyloidosis an...
- nih.gov
It primarily affects individuals of Mediterranean and Middle Eastern ancestry, with symptom onset typically occurring in childhood or young adulthood The condition is characterized by recurrent, self-limiting episodes of fever accompanied by painful serositis involving the peritoneum, pleura, synovium, or skin
- nih.gov
The condition is characterized by recurrent, self-limiting episodes of fever accompanied by painful serositis involving the peritoneum, pleura, synovium, or skin
- medlineplus.gov
Without proper disease control, persistent systemic inflammation can lead to the accumulation of serum amyloid A protein, causing secondary renal amyloidosis and progressive kidney failure
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