C3 glomerulonephritis with genetically confirmed C3 deficiency in a pediatric patient: a case report

• Main Authors: Hae Min Kim (Author), Jae Il Shin (Author), Ji Hong Kim (Author), Jiyoung Oh (Author), Ji-Man Kang (Author), Hee Gyung Kang (Author), Seong Heon Kim (Author), Byoung Soo Cho (Author), Keum Hwa Lee (Author)
• Format: Book
• Published: Korean Society of Pediatric Nephrology, 2024-10-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Complement component 3 glomerulonephritis (C3GN) is a rare kidney disease characterized by complement dysregulation that results in prominent complement component 3 (C3) deposition in the kidneys. The clinical course of C3GN varies from mild hematuria to progressive chronic kidney disease. In most p...