C3 glomerulonephritis with genetically confirmed C3 deficiency in a pediatric patient: a case report
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...
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| Main Authors: | , , , , , , , , |
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| Format: | Book |
| Published: |
Korean Society of Pediatric Nephrology,
2024-10-01T00:00:00Z.
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