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Article

Hypomagnesemia due to two novel TRPM6 mutations.

Journal of pediatric endocrinology & metabolism : JPEM - 1 Nov 2015

Coulter Michelle, Colvin Caroline, Korf Bruce, Messiaen Ludwine, Tuanama Benjamin, Crowley Michael, Crossman David K, McCormick Kenneth

Abstract excerpt

BACKGROUND: Although most hypocalcemia with hypomagenesemia in the neonatal period is due to transient neonatal hypoparathyroidism, magnesium channel defects should also be considered. CASE: We report a case of persistent hypomagnesemia in an 8-day-old Hispanic male who presented with generalized seizures. He was initially found to have hypomagnesemia, hypocalcemia, hyperphosphatemia and normal parathyroid...

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Topics

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Share to Hypocalcemia
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant, Newborn

Share to Magnesium

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Share to Renal Tubular Transport, Inborn Errors

Share to TRPM Cation Channels

Source

Identifiers

PMID: 26226117
DOI: 10.1515/jpem-2014-0394

Genes

TRPM6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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