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Predictors of kidney survival in children with autosomal recessive polycystic kidney disease.

Clinical and experimental nephrology - 1 Mar 2026

Çiçek Neslihan, Gökçe İbrahim, Alavanda Ceren, Güven Serçin, Kaya Mehtap, Pul Serim, Türkkan Özde Nisa, Yıldız Nurdan, Ata Pınar

Abstract excerpt

BACKGROUND: The phenotype of autosomal recessive polycystic kidney disease (ARPKD) can be quite variable: some patients progress to end-stage kidney disease (ESKD) in infancy, while others may not require kidney replacement therapy (KRT) until later childhood or adolescence. This study aimed to evaluate clinical, biochemical, imaging, and genetic findings that may influence kidney prognosis in pediatric patients...

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PMID: 41420720
DOI: 10.1007/s10157-025-02801-w

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