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Renal tubular dysgenesia at the Pereira Rossell Children Hospital
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Keywords

Congenital abnormalities
Renal tubules
Oligohydramnios
Renal Insufficiency
Newborn

How to Cite

Cordobez, R., Lucas, L., Dendi, A., & Moraes, M. (2020). Renal tubular dysgenesia at the Pereira Rossell Children Hospital. Archives of Pediatrics of Uruguay, 91(4), 231–236. https://doi.org/10.31134/ap.91.4.5

Abstract

Renal tubular dysgenesis is an acquired or inherited autosomal recessive disease. Before birth, it shows as oligohydramnios resulting from fetal anuria and after birth, it shows as persistent anuria, pulmonary hypoplasia, severe refractory hypotension and alteration of the ossification of the cranial bones. Histologically, it is an alteration of the development of the renal tubules. We hereby introduce a clinical case of a newborn who presented renal failure, multiple dysmorphia and pulmonary hypoplasia at birth, who died at 3 days of age and whose autopsy showed renal tubular dysgenesis.

https://doi.org/10.31134/ap.91.4.5
pdf (Español (España))
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This work is licensed under a Creative Commons Attribution 4.0 International License.

Copyright (c) 2020 Regina Cordobez, Leandro Lucas, Alvaro Dendi, Mario Moraes

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