Evidence map›Paper›PMID 37576793›Full record

ArticleBalkan journal of medical genetics : BJMG2023

Features of the Wolf-Hirschhorn Syndrome (WHS) from Infant to Young Teenager.

D E Popescu, D Marian, M Zeleniuc, Ch Samoila, V Belengeanu

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PubMed Full text at PMC Publisher
In one paragraph

Article in Balkan journal of medical genetics : BJMG, 2023. 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
1.6field-weighted citation impact, top 15% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Review
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 at 3 institutions in 1 country.

D E PopescuDepartment of Obstetrics-Gynecology and Neonatology, "Victor Babeș" University of Medicine and Pharmacy, Timișoara, Romania.
D MarianDepartment of Operative Dentistry, Faculty of Dental Medicine - "Vasile Goldiş" Western University of Arad, Romania.
M ZeleniucDepartment of Medical Genetics, "Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania.
Ch SamoilaDental Office Dr Samoila Christian, Timişoara, Romania.
V BelengeanuDepartment of Medical Genetics, Faculty of General Medicine, "Vasile Goldiş" Western University of Arad, Romania.
Vasile Goldis Western University of Arad · ROCarol Davila University of Medicine and Pharmacy · ROVictor Babeș University of Medicine and Pharmacy Timișoara · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wolf-Hirschhorn syndrome is a rare condition caused by terminal deletions, of variable size, in the short arm of chromosome 4. The syndrome displays the combination of typical morphological facial variations, intellectual disability, language delay, and various malformations. This report describes the clinical aspect and developmental evolution of a male patient with Wolf-Hirschhorn syndrome, from infancy to adolescence. The patient was first examined and diagnosed at 11 months, with follow-up at the ages of 4 and 16.

Indexed as

Fluorescent in situ hybridization (FISH)PhenotypeSevere delay speechWolf-Hirschhorn syndrome (WHS)

Identifiers

PMID37576793
PMCPMC10413881
OpenAlexW4385730154

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.