Hematuria and proteinuria in pediatric patients can be indicative of various renal pathologies, necessitating a structured diagnostic approach. This case study examines a 9-year-old male presenting with dark-colored urine, mild facial puffiness, and fatigue. Urinalysis revealed significant hematuria with dysmorphic RBCs and proteinuria, prompting further investigations. Laboratory findings, including low C3 levels and elevated ASO titers, led to a diagnosis of Post-Streptococcal Glomerulonephritis (PSGN). The case underscores the importance of early detection, targeted investigations, and supportive management in ensuring positive clinical outcomes.
This study does not involve data sharing.
All authors confirm that there are no conflicts of interest associated with this research.
The sole responsibility for the study design, data gathering, results analysis, and manuscript drafting lies with the author.
No specific grants from any funding agencies in the public, commercial, or non-profit sectors were received for this research, authorship, or publication.
No particular software or tools were employed in this study.
I express my gratitude to those who provided expertise and assistance throughout this study and manuscript preparation. Special thanks to the anonymous peer reviewers for their valuable feedback.
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