Early Urinary Biomarkers in Pediatric Autosomal Dominant Polycystic Kidney Disease (ADPKD): No Evidence in the Interest of Urinary Neutrophil Gelatinase-Associated Lipocalin (uNGAL)

Early Urinary Biomarkers in Pediatric Autosomal Dominant Polycystic Kidney Disease (ADPKD): No Evidence in the Interest of Urinary Neutrophil Gelatinase-Associated Lipocalin (uNGAL)

Background: Autosomal Dominant Polycystic Kidney Disease (ADPKD) is increasingly diagnosed during childhood by the presence of renal cysts in patients with a positive familial history. No curative treatment is available and early detection and diagnosis confronts pediatricians with the lack of early...

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Bibliographic Details
Main Authors: Marianthi Tsingos, Laura Merlini, Marco Solcà, Alexandra Goischke, Alexandra Wilhelm-Bals, Paloma Parvex
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-03-01
Series:Frontiers in Pediatrics
Subjects:
ADPKD
uNGAL
children
renal impairment
TKV
Online Access:https://www.frontiersin.org/article/10.3389/fped.2019.00088/full

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https://www.frontiersin.org/article/10.3389/fped.2019.00088/full

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