Evidence map›Paper›PMID 36150723›Full record

ArticleBMJ case reports2022

Young adolescent with trisomy 13.

Britt C E Kramer, Najma S Abdullahi, Loekie C Ten Have, Annette P M van den Elzen

Open access · greenAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in BMJ case reports, 2022. 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
1.1field-weighted citation impact, top 20% 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, 3 citations in OpenAlex.

  1. Article
  2. Congenital uterine anomalies and congenital heart disease: An underappreciated association?International journal of cardiology. Congenital heart disease · 2025
    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 at 2 institutions in 1 country.

Britt C E KramerPediatrics, Reinier de Graaf Gasthuis, Delft, The Netherlands.
Najma S AbdullahiPediatrics, Erasmus MC, Sophia Childrens Hospital, Rotterdam, The Netherlands.
Loekie C Ten HavePediatrics, Reinier de Graaf Gasthuis, Delft, The Netherlands.
Annette P M van den ElzenPediatrics, Reinier de Graaf Gasthuis, Delft, The Netherlands a.vandenelzen@rdgg.nl.
Reinier de Graaf Hospital · NLErasmus MC - Sophia Children’s Hospital · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A young adolescent girl with trisomy 13 was admitted twice to the paediatric department: the first time because of haematocolpos due to uterus didelphys and unilateral transverse vaginal septum, and the second time because of heart failure due to ruptured sinus of Valsalva aneurysm. As a consequence of the historical early high mortality rate in trisomy 13, we are not aware of known complications in older patients. With better survival nowadays through childhood, we advise structural ultrasonographic cardiac and female genital screening in trisomy 13 patients reaching adolescent age.

Indexed as

Aortic RuptureHematocolposSinus of ValsalvaUrogenital AbnormalitiesAdolescentAgedChildFemaleHumansTrisomy 13 SyndromeUterusCardiovascular medicineCongenital disordersDevelopmental paediatrocsObstetrics and gynaecologyPaediatrics

Identifiers

PMID36150723
PMCPMC9511538
OpenAlexW4296817701

What OpenQuestion holds

Textmetadata
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.