Is C1q nephropathy associated with a WDR19 gene mutation? A case report
HIPPOKRATIA, cilt.25, sa.2, ss.87-90, 2021 (SCI-Expanded, Scopus)
- 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.