Familial Mediterranean fever associated pyrin mutations in Greece
AuthorPrint Email Konstantopoulos, Konstantinos
Constantinou-Deltas, Constantinos D.
Tzioufas, A. G.
Moutsopoulos, H. M.
SourceAnnals of the Rheumatic Diseases
Google Scholar check
MetadataShow full item record
Objective: To search for pyrin mutations associated with familial Mediterranean fever (FMF) in Greece. Patients and methods: 62 patients fulfilling the Tel Hashomer diagnostic criteria for definite (33) or probable (29) FMF diagnosis were studied. Eight point mutations of pyrin gene were tested by standard methods. Of the 62 patients tested, 48 were Greek, four were Jewish, seven were Armenian, and three were Arab. Results: 42 patients were found to be homozygotes for pyrin mutations11 patients were found to carry only one of the tested mutationsin nine patients no mutations were detected. Conclusion: Molecular detection of pyrin gene mutations seems useful in confirming suspected cases, and in detecting asymptomatic cases, of Mediterranean fever in Greece. It may also be used as a screening tool within affected families.