Is C1q nephropathy associated with a WDR19 gene mutation? A case report

KAYNAR R. K., GÜVERCİN B., Gueler O., Mungan S., ÇAĞLAYAN E.

HIPPOKRATIA, cilt.25, sa.2, ss.87-90, 2021 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 25 Sayı: 2
  • Basım Tarihi: 2021
  • Dergi Adı: HIPPOKRATIA
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, EMBASE
  • Sayfa Sayıları: ss.87-90
  • Anahtar Kelimeler: Complement C1q, glomerulonephritis, proteinuria
  • Karadeniz Teknik Üniversitesi Adresli: Evet

Özet

Background: Even though complement 1q nephropathy (C1qN) was first introduced in 1985, this entity is still unknown and recognized by clinicians due to its rare prevalence (0.2 - 2.5 %) and insufficient emphasis.