Evidence map›Paper›PMID 30656008›Full record

ArticleClinical case reports2019

Variable phenotypic expression of Apert syndrome in monozygotic twins.

Matthieu Dap, Pascale Bach-Segura, Charline Bertholdt, Didier Menzies, Jean-Pierre Masutti, Olivier Klein, Estelle Perdriolle-Galet, Laetitia Lambert, Olivier Morel

Open access · goldAbstract readCase Reports
In one paragraph

Article in Clinical case reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Cleft Palate in Apert Syndrome.Journal of developmental biology · 2022
    Review
  2. Article
  3. 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

9 authors at 2 institutions in 1 country.

Matthieu DapDepartment of Gynecology and Obstetrics CHRU de Nancy Nancy France.ORCID 0000-0002-2846-1509
Pascale Bach-SeguraDepartment of Perinatal Radiology and Imaging CHRU de Nancy Nancy France.
Charline BertholdtDepartment of Gynecology and Obstetrics CHRU de Nancy Nancy France.
Didier MenziesDepartment of Fetopathology CHRU de Nancy Nancy France.
Jean-Pierre MasuttiDepartment of Fetopathology CHRU de Nancy Nancy France.
Olivier KleinDepartment of Pediatric Neurosurgery CHRU de Nancy Nancy France.
Estelle Perdriolle-GaletDepartment of Gynecology and Obstetrics CHRU de Nancy Nancy France.
Laetitia LambertDepartment of Clinical Genetic CHRU de Nancy Nancy France.
Olivier MorelDepartment of Gynecology and Obstetrics CHRU de Nancy Nancy France.
Centre Hospitalier Régional et Universitaire de Nancy · FRImagerie Adaptative Diagnostique et Interventionnelle · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Apert syndrome in monozygotic twins can lead to different phenotypic expression of the disease in the two fetuses. Apert syndrome can be associated with congenital left diaphragmatic hernia and cleft palate.

Indexed as

Apert syndromecongenital diaphragmatic herniacraniosynostosisfetal autopsyfetal ultrasoundmonozygotic twins

Identifiers

PMID30656008
PMCPMC6333066
OpenAlexW2901472652

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.