MEFV gene variants in children with Henoch-Schönlein purpura and association with clinical manifestations: a single-center Mediterranean experience.
Rabia Miray Kisla EkinciSibel BalcıSerdar CeylanerBahriye AtmisDilek KaragozDerya Ufuk AltintasMustafa YilmazPublished in: Postgraduate medicine (2018)
MEFV variants in exon 10 may affect clinical presentation of HSP in populations where FMF is common. While HSP may be an initial symptom of FMF, we speculate that physicians should be aware of FMF possibility in children with intussusception and lower hemoglobin, higher serum IgA, leukocyte, and platelet count.