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Updated: Jul 14, 2026

Isolation, Characterization, And High Throughput Extracellular Flux Analysis of Mouse Primary Renal Tubular Epithelial Cells
Published on: June 20, 2018
[Renal tubular dysgenesis and mutation in the renin gene]
J Bacchetta1, F Dijoud, R Bouvier
1Centre de référence des maladies rénales héréditaires, département de pédiatrie, hôpital Edouard-Herriot et université Claude-Bernard-Lyon-I, 69437 Lyon cedex 03, France.
Abstract:
Renal tubular dysgenesis is a severe and rare disorder of the renal development characterized by fetal anuria, oligohydramnios and early death from pulmonary hypoplasia and refractory arterial hypotension. We report on a female patient who presented with anuria in the neonatal period, requiring peritoneal dialysis until 5 months of age with unexpected diuresis recovery at 2 months of age. Clinical, histological and pathophysiological issues are discussed for this disease related to a mutation in the renin gene.
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