Evidence map›Paper›PMID 40469581›Full record

ArticleMolecular genetics and metabolism reports2025

X-linked hypohidrotic ectodermal dysplasia associated with gastroesophageal reflux disease.

Yamato Hanawa, Wataru Murasaki, Tatsuya Ando, Yuji Baba, Hiroyuki Namba

Abstract read
In one paragraph

Article in Molecular genetics and metabolism reports, 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.

Yamato HanawaDepartment of Pediatrics, Jikei University Kashiwa Hospital, Chiba, Japan.
Wataru MurasakiDepartment of Pediatrics, Jikei University Kashiwa Hospital, Chiba, Japan.
Tatsuya AndoDepartment of Pediatrics, Jikei University Kashiwa Hospital, Chiba, Japan.
Yuji BabaDepartment of Surgery, Jikei University Kashiwa Hospital, Chiba, Japan.
Hiroyuki NambaDepartment of Pediatrics, Jikei University Kashiwa Hospital, Chiba, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

X-linked hypohidrotic ectodermal dysplasia (XLHED) is a rare genetic congenital disorder characterized by allelic heterogeneity, affecting the ectodermal structures. We present the case of a 4-month-old boy diagnosed with XLHED, suffering from recurrent aspiration pneumonia due to gastroesophageal reflux disease (GERD) since he was 1-month-old. This case highlights that GERD, when severe enough to cause aspiration pneumonia, may be associated with underlying ectodermal dysplasia, such as XLHED. In such cases, tube feeding may reduce the risk of pneumonia in infants with XLHED.

Indexed as

Ectodermal dysplasiaGERDRecurrent pneumoniaXLHED

Identifiers

PMID40469581
PMCPMC12136819

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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.