Article
MEFV gene mutations and clinical course in pediatric patients with Henoch-Schönlein purpura.
Archivos argentinos de pediatria - 1 Jun 2018
Can Emrah, Kılınç Yaprak Zubeyde, Hamilçıkan Şahin, Erol Meltem, Bostan Gayret Y Özgül Yiğit Özlem
Abstract excerpt
OBJECTIVE: To determine the frequency of the MEFV gene mutations in pediatric patients diagnosed with HSP and to assess the effect of the MEFV gene mutations on their prognosis. Material and Methods. Ccross-sectional study; pediatric patients between 2-11 years diagnosed with HSP were included. These cases were investigated for 6 MEFV gene mutations (M694V, M680I, A744S, R202Q, K695R, E148Q). RESULTS: Eighty...
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