Familial Mediterranean Fever
Authors
Abstract
Familial Mediterranean Fever (FMF) or recurrent polyserositis is an inherited multisystem disease manifested by recurrent painful attacks affecting the abdomen, chest or joints, often accompanied by fever and sometimes a skin rash. FMF is a genetic condition, inherited in an autosomal recessive fashions. FMF could be described as a disorder of inappropriate inflammation of one or more of serusal membrane (serositis). The diagnosis of FMF is generally based on the clinical criteria although the direct analysis of MEFV gene is the only method to be certain of the disease. The goals of therapy are to reduce the morbidity and prevent complications of the disease, which is consists of taking colchicine, a neutrophil suppresisive agent. Since FMF is a genetic disease, it can be prevented only if the carriers of the defective gene are identified.
Copyright
© 2006, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.
Similar Articles
Evaluation of Children with Familial Mediterranean Fever in South-Eastern Region of Türkiye
Dogan A, Balat A, Demircioglu Kilic B, Akbalık Kara M, Buyukcelik M. Evaluation of Children with Familial Mediterranean Fever in South-Eastern Region of Türkiye. Inn J Pediatr. 2025;35(1):e148367. doi: https://doi.org/10.5812/ijp-148367
Genetic and Clinical Manifestations of Familial Mediterranean Fever in Children from the Central North of Iran
Maleknejad S, Shabani A, Safaei Asl A, Miremarati A, Safaei-Asl P, et al. Genetic and Clinical Manifestations of Familial Mediterranean Fever in Children from the Central North of Iran. Inn J Pediatr. 2024;34(3):e146276. doi: https://doi.org/10.5812/ijp-146276
The Association of Familial Mediterranean Fever and Polyarteritis Nodosa: A Case Report
Shiari R, Sadat Ahadi H, Farivar S, Sayyahfar S. The Association of Familial Mediterranean Fever and Polyarteritis Nodosa: A Case Report. Arch Pediatr Infect Dis. 2015;3(2):e17469. doi: https://doi.org/10.5812/pedinfect.17469
Genetic and Clinical Study of Children with Familial Mediterranean Fever in Northeastern Iran
Malek A, Abbaszadegan M, Vakili N, Zeraati T, Ghayoor Karimiani E, et al. Genetic and Clinical Study of Children with Familial Mediterranean Fever in Northeastern Iran. J Compr Ped. 2024;15(2):e140025. doi: https://doi.org/10.5812/jcp-140025
MEFV Mutation Frequency in Pediatric Patients with Familial Mediterranean Fever and its Relationship with Clinical Phenotypes in Marmara Region of Turkey
Gok V, Yigit O, Bostan Gayret O, Hamilcikan S. MEFV Mutation Frequency in Pediatric Patients with Familial Mediterranean Fever and its Relationship with Clinical Phenotypes in Marmara Region of Turkey. Inn J Pediatr. 2017;27(3):e10684. doi: https://doi.org/10.5812/ijp.10684
- Scopus by DOI: 0
Last Update: 1 month ago
- Scopus by Title: 6
Last Update: 1 month ago
- Scopus by Title (Ref): 4
Last Update: 1 month ago
- CrossRef: 0
Last Update: 6 days ago