Abstract
The diagnostic work up of C3 Glomerulopathy in resource limited settings remains a challenge and is often incomplete due to either unavailability of assays such as tests for detecting C3 nephritic factor and other abnormalities in alternate complement pathways or lack of access to electron microscopy and genetic testing due to cost. Whether this impacts outcome is unclear. The objective of the study is to describe the clinico-pathological profile of C3G, response to immunosuppression and short-term renal outcomes in children in a resource limited setting.
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