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

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

HIPPOKRATIA, vol.25, no.2, pp.87-90, 2021 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 25 Issue: 2
  • Publication Date: 2021
  • Journal Name: HIPPOKRATIA
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, EMBASE
  • Page Numbers: pp.87-90
  • Keywords: Complement C1q, glomerulonephritis, proteinuria
  • Karadeniz Technical University Affiliated: Yes

Abstract

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.