C3 glomerulopathy in children: experience at a resource-limited center
Pediatric C3G has a variable clinicopathological spectrum, while DDD is less common. Most patients present with glomerulonephritis and significant morbidities. The lack of genetic and C3Nephritic factor testing is a barrier to the comprehensive phenotyping and management of C3G in resource-limited settings.
Authors
- Anil Vasudevan (ORCID: https://orcid.org/0000-0003-4338-0325)
- Mahesha Vankalakunti (ORCID: https://orcid.org/0000-0002-7521-2257)
- Abhishek Ghante
- Soumya Reddy
Institutions
- St. John's National Academy of Health Sciences (IN)
- St.John's Medical College Hospital (IN)
- Manipal Hospital (IN)
Publication Details
- Journal
- Clinical and Experimental Pediatrics
- Published
- 2024-11-28
- DOI
- https://doi.org/10.3345/cep.2024.01256
- Citations
- 1
- Primary Topic
- Complement system in diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.24