Evidence map›Paper›PMID 40535402›Full record

ArticleCureus2025

Autosomal Recessive Becker's Form of Myotonia Congenita in Indian Families.

Sahithi Krovvidi, Srilaxmi Nelakurthi, Mounika Gedela, Srinithya Singamsetty, Vijayalakshmi Bhimireddy

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. 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
–field-weighted citation impact
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.

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

5 authors.

Sahithi KrovvidiInternal Medicine, NRI Medical College and General Hospital, Guntur, IND.
Srilaxmi NelakurthiPediatrics, NRI Medical College and General Hospital, Guntur, IND.
Mounika GedelaPediatrics, NRI Medical College and General Hospital, Guntur, IND.
Srinithya SingamsettyPediatrics, NRI Medical College and General Hospital, Guntur, IND.
Vijayalakshmi BhimireddyPediatrics, NRI Medical College and General Hospital, Guntur, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myotonia congenita (MC), a rare inherited disease, is caused by variations in the skeletal muscle chloride voltage-gated channel one gene (

Indexed as

becker’s diseaseclcn1 genemutationmyotonia congenitanon-dystrophic myotonia

Identifiers

PMID40535402
PMCPMC12176253

What OpenQuestion holds

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LicenceCC BY
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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.