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Article

Hypomagnesemia is underestimated in children with HNF1B mutations.

Pediatric nephrology (Berlin, Germany) - 1 Oct 2020

Kołbuc Marcin, Leßmeier Lennart, Salamon-Słowińska Dorota, Małecka Ilona, Pawlaczyk Krzysztof, Walkowiak Jarosław, Wysocki Jacek, Beck Bodo B, Zaniew Marcin

Abstract excerpt

BACKGROUND: Hypomagnesemia in patients with congenital anomalies of the kidneys and urinary tract or autosomal dominant tubulointerstitial kidney disease is highly suggestive of HNF1B-associated disease. Intriguingly, the frequency of low serum Mg2+ (sMg) level varies and is lower in children than in adults with HNF1B mutations that could be partially due to application of inaccurate normal limit of sMg,...

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PMID: 32388583
DOI: 10.1007/s00467-020-04576-6

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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