Evidence map›Paper›PMID 42147080›Full record

ArticleJCEM case reports2026

Thyroid dyshormonogenesis caused by iodotyrosine deiodinase pathogenic variant: three cases presenting in adolescence.

Isabelle En Xin Choong, Suet Ching Chen, Mohamad Guftar Shaikh

Abstract readCase Reports
In one paragraph

Article in JCEM case reports, 2026. 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

3 authors.

Isabelle En Xin ChoongDevelopmental Endocrinology Research Group, University of Glasgow, Glasgow G12 8QQ, UK.ORCID https://orcid.org/0000-0003-2247-7056
Suet Ching ChenDevelopmental Endocrinology Research Group, University of Glasgow, Glasgow G12 8QQ, UK.ORCID https://orcid.org/0000-0002-2866-6360
Mohamad Guftar ShaikhDevelopmental Endocrinology Research Group, University of Glasgow, Glasgow G12 8QQ, UK.ORCID https://orcid.org/0000-0002-2316-3334

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We describe three patients from three unrelated consanguineous families, all homozygous for the c.301C>T (p.Arg101Trp) variant in the iodotyrosine deiodinase

Indexed as

congenital hypothyroidismgeneticsiodotyrosine deiodinase (IYD) genelevothyroxinethyroid dyshormonogenesis

Identifiers

PMID42147080
PMCPMC13171439

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.