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Patient management and the association of less common familial Mediterranean fever symptoms with other disorders
Author(s) -
Mike M. Moradian,
Tamara Sarkisian,
Gayane Amaryan,
Hasmik Hayrapetyan,
Anna Yeghiazaryan,
Nairi Davidian,
Nare Avanesian
Publication year - 2013
Publication title -
genetics in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.509
H-Index - 128
eISSN - 1530-0366
pISSN - 1098-3600
DOI - 10.1038/gim.2013.112
Subject(s) - familial mediterranean fever , mefv , medicine , oligoarthritis , sacroiliitis , serositis , arthritis , dermatology , penetrance , amyloidosis , pediatrics , polyarthritis , gene mutation , mutation , genetics , disease , biology , gene , phenotype
In this study, we present clinical data from 16,000 familial Mediterranean fever patients. We also discuss the clinical manifestation of a subset of these patients and their potential symptom associations with other disorders.

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