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Objective. FMF is an autosomal recessive hereditary disease, associated with a single gene named MEFV. This gene is considered to be responsible only for FMF. In the present study, we tried to find out whether the MEFV gene is associated with or responsible for clinical conditions other than FMF. Methods. We looked for patients who presented with signs and symptoms not typical for FMF but carried MEFV mutations. We also searched for reports about similar conditions in the English medicaldoi:10.1093/rheumatology/kep296 pmid:19837680 fatcat:w4cyd5qo7jdaxo27wozhifs6n4