Abstract
Congenital nephrotic syndrome (CNS) is a rare glomerular disease characterized by massive proteinuria, hypoproteinemia, and generalized edema that manifests in the first 3 months of life. This report describes the case of a patient with congenital nephrotic syndrome secondary to congenital infection in a pediatric patient. The article aims to sensitize pediatricians to the pathology and its etiologies, considering that clinical suspicion allows for better therapeutic management of affected patients and the prevention of potential sequelae.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Paper version not known
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
