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[RENAL TUBULAR DYSGENESIS SECONDARY TO MUTATIONS IN GENES ENCODING THE RENIN-ANGIOTENSIN SYSTEM].

Harefuah - 1 Dec 2021

Schreiber Ruth, Dolgin Vadim, Landau Daniel, Gurevich Evgenia, Shalev Hanna, Geylis Michael

Abstract excerpt

INTRODUCTION: Autosomal recessive renal tubular dysgenesis (RTD;OMIM: 267430) is a rare kidney disease secondary to mutations in genes encoding the renin-angiotensin system which have a role in renal tissue development during fetal life and in the maintenance of blood pressure and electrolyte balance. The disease is characterized by oligohydramnios, prematurity, neonatal renal failure, hypotension and...

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PMID: 34957720

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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