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-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 131 Sayı: 1
  • Basım Tarihi: 2019
  • Doi Numarası: 10.1080/00325481.2019.1552479
  • Dergi Adı: POSTGRADUATE MEDICINE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.68-72
  • Anahtar Kelimeler: Genetics, Henoch-Schonlein purpura, IgA vasculitis, MEFV, MUTATIONS, FEVER, PREVALENCE, VASCULITIS, CLASSIFICATION, CRITERIA, DISEASES, TURKEY, FMF
  • Çukurova Üniversitesi Adresli: Evet

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.