Evidence map›Paper›PMID 38567178›Full record

ArticleJournal of pediatric genetics2024

Hypomagnesemia with Secondary Hypoparathyroidism and Hypocalcemia due to Novel Variants in the Transient Receptor Potential Cation Channel Subfamily M Member 6 (

Geetanjali Jain, Gourab Das, Rakhi Malhotra, Sateesh Ramchandran, Nagaraja M Phani, Giridharan Appaswamy, Upasana Sridharan, Aradhana Dwivedi

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PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of pediatric genetics, 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
0.1field-weighted citation impact, top 55% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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, 1 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

8 authors at 1 institution in 1 country.

Geetanjali JainMilitary Hospital, Nasirabad, India.
Gourab DasArmy Hospital (Research and Referral), New Delhi, India.
Rakhi MalhotraDepartment of Endocrinology, Army Hospital (Research and Referral), New Delhi, Delhi, India.
Sateesh RamchandranDepartment of Endocrinology, Army Hospital (Research and Referral), New Delhi, Delhi, India.
Nagaraja M PhaniDepartment of Molecular Genetics, Life cell Diagnostics Pvt. Ltd., India.
Giridharan AppaswamyLife Cell Diagnostic Pvt. Ltd., Chennai, Tamil Nadu, India.
Upasana SridharanLife Cell Diagnostic Pvt. Ltd., Chennai, Tamil Nadu, India.
Aradhana DwivediDepartment of Pediatrics, Division of Clinical Genetics, Army Hospital (Research and Referral), New Delhi, India.
Army Hospital Research and Referral · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HOMG1 (hypomagnesemia 1, intestinal) or hypomagnesemia with secondary hypocalcemia is a rare autosomal recessive disorder of magnesium metabolism, characterized by impaired magnesium absorption. This disorder may mimic other conditions presenting with neonatal seizures. Here, we report an infant diagnosed to have hypomagnesemia with secondary hypocalcemia due to novel variants in

Indexed as

hypocalcemiahypomagnesemiahypoparathyroidismTRPM6

Identifiers

PMID38567178
PMCPMC10984712
OpenAlexW3198186892

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.