Skip to main content
Annals of the Rheumatic Diseases logoLink to Annals of the Rheumatic Diseases
. 2003 May;62(5):479–481. doi: 10.1136/ard.62.5.479

Familial Mediterranean fever associated pyrin mutations in Greece

K Konstantopoulos 1, A Kanta 1, C Deltas 1, V Atamian 1, D Mavrogianni 1, A Tzioufas 1, I Kollainis 1, K Ritis 1, H Moutsopoulos 1
PMCID: PMC1754548  PMID: 12695165

Abstract

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 mutations; 11 patients were found to carry only one of the tested mutations; in 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.

Full Text

The Full Text of this article is available as a PDF (120.5 KB).


Articles from Annals of the Rheumatic Diseases are provided here courtesy of BMJ Publishing Group

RESOURCES