Evidence map›Paper›PMID 30214764›Full record

ArticleClinical case reports2018

Congenital diaphragmatic hernia in a case of Cat eye syndrome.

Ebru Aileen Alsat, Heiko Reutter, Soyhan Bagci, Florian Kipfmueller, Hartmut Engels, Ruth Raff, Elisabeth Mangold, Ulrich Gembruch, Annegret Geipel, Andreas Müller and 1 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Clinical case reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. 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

11 authors at 2 institutions in 1 country.

Ebru Aileen AlsatDepartment of Neonatology and Pediatric Intensive Care University of Bonn Bonn Germany.ORCID 0000-0002-5805-1922
Heiko ReutterDepartment of Neonatology and Pediatric Intensive Care University of Bonn Bonn Germany.
Soyhan BagciDepartment of Neonatology and Pediatric Intensive Care University of Bonn Bonn Germany.
Florian KipfmuellerDepartment of Neonatology and Pediatric Intensive Care University of Bonn Bonn Germany.
Hartmut EngelsInstitute of Human Genetics University of Bonn Bonn Germany.
Ruth RaffInstitute of Human Genetics University of Bonn Bonn Germany.
Elisabeth MangoldInstitute of Human Genetics University of Bonn Bonn Germany.
Ulrich GembruchDepartment of Obstetrics and Prenatal Medicine University of Bonn Bonn Germany.
Annegret GeipelDepartment of Obstetrics and Prenatal Medicine University of Bonn Bonn Germany.
Andreas MüllerDepartment of Neonatology and Pediatric Intensive Care University of Bonn Bonn Germany.
Thomas SchaibleDepartment of Neonatology University Medicine Mannheim University of Heidelberg Mannheim Germany.
University of Bonn · DETechnische Hochschule Mannheim · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our findings extend the phenotypic spectrum of Cat eye syndrome, a disorder with wide clinical variability. The potentially life-threatening complications of congenital diaphragmatic hernia should be considered in genetic counseling and prenatal diagnostic.

Indexed as

22q11.2case reportCat eye syndromecongenital diaphragmatic herniasupernumerary bisatellited marker chromosome

Identifiers

PMID30214764
PMCPMC6132134
OpenAlexW2883261374

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.