Evidence map›Paper›PMID 38528672›Full record

ArticleThe American journal of case reports2024

A Rare Case of Neonatal Hypomagnesemia with Secondary Hypocalcemia Caused by a Novel Homozygous TRPM6 Gene Variant.

Mohammed Shahab Uddin, AlZahra Y Alradhi, Fahad Mushbb N Alqathani, Othman Saleh Alessa, Ahmed Nawfal M Alshammari, Ratna Tripathy, Mohammed Ahmed Alomari

Open access · hybridAbstract readCase Reports
In one paragraph

Article in The American journal of case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
1.2field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Mohammed Shahab UddinDepartment of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia.ORCID 0000-0001-7372-4796
AlZahra Y AlradhiDepartment of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia.ORCID 0000-0001-7854-0099
Fahad Mushbb N AlqathaniDepartment of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia.ORCID 0009-0007-0195-717X
Othman Saleh AlessaDepartment of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia.ORCID 0009-0002-0700-7785
Ahmed Nawfal M AlshammariDepartment of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia.ORCID 0000-0003-3217-4796
Ratna TripathyDepartment of Human Genetics, Bioscientia Institute for Medical Diagnostics GmbH, Ingelheim, Germany.
Mohammed Ahmed AlomariDepartment of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia.
National Guard Health Affairs · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Familial hypomagnesemia with secondary hypocalcemia (HSH) is a rare autosomal recessive disorder (OMIM# 602014) caused by mutations in the gene encoding transient receptor potential melastatin 6 (TRPM6)) on chromosome 9q22, a channel involved in epithelial magnesium resorption. While a plethora of studies have delineated various clinical manifestations pertinent to this mutation, the literature is devoid of connections between TRPM6 mutations and bleeding diathesis, or sudden infant death syndrome (SIDS). This report presents a case of familial HSH associated with the novel homozygous TRPM6 gene variant c.5281C>G p. (Arg1761Gly) chr9: 77354845. CASE REPORT This report details a 26-day-old neonate, born full term with optimal Apgar scores, who experienced an abrupt emergence of apnea, cyanosis, bilateral nasal bleeding, and diminished alertness. Despite the neonate's initially unremarkable clinical birth indicators, a meticulous assessment unveiled a pronounced family history of SIDS, including a sibling previously diagnosed with hypomagnesemia. Laboratory examination of the infant demonstrated severe hypomagnesemia and hypocalcemia, conditions which were promptly ameliorated following intravenous administration of magnesium and calcium. Whole-exome sequencing identified a homozygous TRPM6 gene mutation c.5281C>G p. (Arg1761Gly) at chr9: 77354845. This gene is crucial for magnesium regulation. The mutation involves a cytosine-to-guanine shift, resulting in an arginine to glycine amino acid substitution at position 1761 of the TRPM6 protein. CONCLUSIONS This report has highlighted that infantile hypomagnesemia may be associated with symptoms and signs that can mimic infection, or it can present with seizures. Although familial HSH is a rare genetic disorder that can be identified by genetic testing, correction of hypomagnesemia is the most important and immediate clinical management strategy.

Indexed as

HypocalcemiaMagnesium DeficiencySudden Infant DeathTRPM Cation ChannelsHumansInfantInfant, NewbornMagnesiumMagnesiumTRPM6 protein, humanTRPM Cation Channels

Identifiers

PMID38528672
PMCPMC10985420
OpenAlexW4392284699

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.