A case report: 19-year-old male diagnosed with C1q nephropathy requiring renal replacement therapy
C1q nephropathy is a rare glomerular disease. Clinical presentation is diverse and ranges from asymptomatic hematuria or proteinuria to symptoms and signs of nephrotic/nephritic syndrome. On light microscopy, it can be classified into two subtypes: minimal change disease (MCD)/focal segmental glomer...
Main Authors: | Randa Choueiri, Joelle Faddoul, Claude Ghorra, Jaqueline Al Najjar, Beatrice-Blondine Akiki, Sora Boustany, Vanessa Nseir |
---|---|
Format: | Article |
Language: | English |
Published: |
Open Exploration Publishing Inc.
2022-08-01
|
Series: | Exploration of Medicine |
Subjects: | |
Online Access: | https://www.explorationpub.com/Journals/em/Article/1001101 |
Similar Items
-
Diagnosing Fabry nephropathy: the challenge of multiple kidney disease
by: Pasquale Esposito, et al.
Published: (2023-11-01) -
Management of IgA Nephropathy in Pediatric Patients
by: Sophie Schroda, et al.
Published: (2022-05-01) -
Morphological pattern of non-diabetic nephropathy in type 2 diabetes mellitus patients
by: Meral Mese, et al.
Published: (2022-06-01) -
Acute kidney injury in patients with idiopathic membranous nephropathy: influencing factors and prognosis
by: Zhenzhou Li, et al.
Published: (2023-12-01) -
Validation of IgA nephropathy diagnosis in the Swedish Renal Registry
by: Johanna Rehnberg, et al.
Published: (2024-03-01)