Paediatric Nephrotic Syndrome at Gabriel Touré University Hospital, Mali: A 30-Month Cross-Sectional Study
Traoré Kalirou, Sacko Karamoko, Maiga Belco, Konaré Hawa, Konaté Djeneba, Dembélé Adama, Touré Amadou, Traoré Fousseyni, Koné Salia, Dembélé Hawa, Cissé Mohamed Elmouloud, Coulibaly Oumar, Togo Pierre, Doumbia Abdoul Karim, Maiga Leyla, Sidibé Lala N’drainy, Doumbia Aminata, Ouattara Arouna, Traore Bory, Diarra Mohamed, Coulibaly Yacouba, Simaga Tati, Sangaré Aboubacar, Diarra Lassina, Diakité Abdoul Aziz, Dicko Fatoumata, Togo Boubacar, Sylla Mariam
Asian Journal of Pediatric Research · pp. 9–15 · Published 18 Nov 2025
10.9734/ajpr/2025/v15i12491Abstract
Introduction: Nephrotic syndrome (NS) is biologically defined by hypoalbuminemia below 30 g/L and proteinuria above 50 mg/kg/day or above 200 g/mol of urinary creatinine in a sample. It is one of the most common glomerular nephropathies occurring in children between the ages of 2 and 7, often following an infectious or allergic trigger. Materials and Methods: We conducted a cross-sectional study over a 30-month period from January 1, 2018, to June 30, 2020, among children aged 0 to 15 years admitted to the pediatric department of the Gabriel TOURE University Hospital for nephrotic syndrome. Results: Over the 30-month period, we collected 65 files that met the inclusion criteria out of a total of 19,047 hospitalizations, representing a hospitalization rate of 0.34%. The average age was 7.15 ± 3.92, with extremes ranging from 1 to 14 years. The sex ratio was 2.82. Twenty-four-hour proteinuria was between 100 and 200 mg/kg/day in 64.6% of cases, and 4.7% had proteinuria greater than 300 mg/kg/day. All children received corticosteroid therapy. Conclusion: NS is the most common kidney disease in children. Early treatment with corticosteroids and rigorous follow-up are essential, but remain difficult to implement in resource-limited settings.
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