Case Report: effect of lumasiran treatment in a late preterm baby with antenatal diagnosis of primary hyperoxaluria type 1

BackgroundPrimary hyperoxaluria type 1 (PH1) is a rare disease with autosomal recessive transmission, characterized by increased urinary excretion of oxalate, resulting in chronic kidney disease secondary to recurrent urolithiasis, nephrocalcinosis, and accumulation of oxalate in various organs and...

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Bibliographic Details

Published in:	Frontiers in Pediatrics
Main Authors:	Francesca Taroni, Alfredo Berrettini, Michele Gnech, Francesca Rella, Gian Antonio Manzoni, Giovanni Montini
Format:	Article
Language:	English
Published:	Frontiers Media S.A. 2024-01-01
Subjects:	late preterm lumasiran newborn prenatal diagnosis primary hyperoxaluria type 1
Online Access:	https://www.frontiersin.org/articles/10.3389/fped.2023.1338909/full