MEFV Mutations Modify the Clinical Presentation of Henoch-Schonlein Purpura

Date
2008
Author
Uncu, Nermin
Kasapcopur, Oezguer
Kara, Nazli
Ekim, Mesiha
Arisoy, Nil
Ozcakar, Z. Birsin
Yalcinkaya, Fatos
Cakar, Nilguen
Acar, Banu
Uguten, Deniz
Soy, Derya
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Abstract
Objective. To investigate the prevalence of MEFV gene mutations in Turkish patients with Henoch-Schonlein purpura (HSP) but with no symptoms of familial Mediterranean fever (FMF). In addition, we assessed the clinical and laboratory characteristics of HSP patients with and without MEFV mutations.
URI
http://hdl.handle.net/20.500.12627/89826
https://doi.org/10.3899/jrheum.080405
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