P01-028 – MEFV mutation in Morrocan child wuth familial Mediterranean fever.

Familial Mediterranean Fever ( FMF ) is an autosomal recessive inherited disease mostly wide spread in the Mediterranean basin. It is manifested by a fever associated with paroxystic painful attacks. The prognosis is determined by the occurrence of renal amyloidosis. The purpose of our work is to establish a genotype- phenotype correlation between the MEFV gene mutation and the expression of the FMF in 10 Moroccan children.