Expanding the clinical spectrum of autosomal‐recessive renal tubular dysgenesis: Two siblings with neonatal survival and review of the literature

Expanding the clinical spectrum of autosomal‐recessive renal tubular dysgenesis: Two siblings with neonatal survival and review of the literature

Abstract Background Autosomal‐recessive renal tubular dysgenesis (AR‐RTD) is a rare genetic disorder caused by defects in the renin‐angiotensin system that manifests as fetal anuria leading to oligohydramnios and Potter sequence. Although the most common outcome is neonatal death from renal failure,...

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Bibliographic Details
Main Authors: Krista M. Vincent, Afrah Alrajhi, Joanna Lazier, Brigitte Bonin, Sarah Lawrence, Gabrielle Weiler, Christine M. Armour
Format: Article
Language:English
Published: Wiley 2022-05-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
fludrocortisone
renal tubular dysgenesis
survival
Online Access:https://doi.org/10.1002/mgg3.1920

Internet

https://doi.org/10.1002/mgg3.1920

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