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Article

Bartter syndrome prenatal diagnosis based on amniotic fluid biochemical analysis.

Pediatric research - 1 Mar 2010

Garnier Arnaud, Dreux Sophie, Vargas-Poussou Rosa, Oury Jean-François, Benachi Alexandra, Deschênes Georges, Muller Françoise

Abstract excerpt

Bartter syndrome is an autosomic recessive disease characterized by severe polyuria and sodium renal loss. The responsible genes encode proteins involved in electrolyte tubular reabsorption. Prenatal manifestations, mainly recurrent polyhydramnios because of fetal polyuria, lead to premature deli...

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Identifiers

PMID: 19915517
DOI: 10.1203/PDR.0b013e3181ca038d

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19915517-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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