Evidence map›Paper›PMID 41458703›Full record

ArticleCureus2025

Harlequin Ichthyosis in a Preterm Neonate: A Case Report.

Alexandra Maria Ulmeanu, Diana Maria Damian, Roxana Maria Nemes, Cristina Aurelia Ionita

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. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

4 authors.

Alexandra Maria UlmeanuNeonatology, Regina Maria Hospital, Bucharest, ROU.
Diana Maria DamianNeonatology, Regina Maria Hospital, Bucharest, ROU.
Roxana Maria NemesPulmonology Department, University Titu Maiorescu, Bucharest, ROU.
Cristina Aurelia IonitaNeonatology, Regina Maria Hospital, Bucharest, ROU.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Harlequin ichthyosis is a rare autosomal recessive disorder characterized by severe hyperkeratosis and impaired skin barrier function, often associated with high neonatal mortality. We present the case of a preterm neonate born by cesarean section at 32 weeks of gestation with classical features of Harlequin ichthyosis, confirmed by genetic testing. Despite intensive neonatal and dermatologic management, the patient developed multiorgan complications and died on the 30th day of life. This report emphasizes the importance of early diagnosis, supportive care, and genetic counseling for affected families.

Indexed as

genetic disorderharlequin ichthyosisneonateprematuritysurfactant deficiency

Identifiers

PMID41458703
PMCPMC12743277

What OpenQuestion holds

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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.