MEW gene variants in children with Henoch-Schonlein purpura and association with clinical manifestations: a singie-center Mediterranean experience


Ekinci R. M. , Balci S. , Bisgin A. , Atmis B. , Dogruel D. , Altintas D. U. , ...Daha Fazla

POSTGRADUATE MEDICINE, cilt.131, sa.1, ss.68-72, 2019 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 131 Konu: 1
  • Basım Tarihi: 2019
  • Doi Numarası: 10.1080/00325481.2019.1552479
  • Dergi Adı: POSTGRADUATE MEDICINE
  • Sayfa Sayıları: ss.68-72

Özet

Objectives: Henoch-Schonlein purpura (HSP) is characterized by non-thrombocytopenic palpable purpura, abdominal pain, and arthralgia/arthritis. We aimed to describe the clinical presentations of children with HSP in a single center and compare the prevalence of each manifestations between patients with MEFV variants, particularly in exon 10 and those without.