Evidence map›Paper›PMID 30081864›Full record

ReviewBMC pediatrics2018

Mosaicism trisomy 10 in a 14-month-old child with additional neurological abnormalities: case report and literature review.

Yang Gao, Yu-Cong Ma, Yang-Hua Ju, Ya-Nan Li

Open access · goldAbstract readCase ReportsReview
PubMed Full text at PMC Publisher
In one paragraph

Review in BMC pediatrics, 2018. 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
1.1field-weighted citation impact, top 18% 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, 6 citations in OpenAlex.

  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 at 2 institutions in 1 country.

Yang GaoDepartment of Pediatrics, The First Hospital of Jilin University, Changchun, Jilin, 130021, People's Republic of China.
Yu-Cong MaDepartment of Pediatrics, The First Hospital of Jilin University, Changchun, Jilin, 130021, People's Republic of China.
Yang-Hua JuDepartment of Pediatrics, The First Hospital of Jilin University, Changchun, Jilin, 130021, People's Republic of China.
Ya-Nan LiDepartment of Pediatrics, The First Hospital of Jilin University, Changchun, Jilin, 130021, People's Republic of China. lyanan2008@sina.com.
First Hospital of Jilin University · CNJilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTrisomy 10 is very rarely diagnosed, especially in living persons. Most reports of trisomy 10 pertain to prenatal diagnosis of trisomy 10 in the fetus. In addition, trisomy 10 has been reported as part of partial chromosomal abnormalities in some leukemic cells and tumor specimens. Only 6 cases of mosaicism trisomy 10 have been reported so far. None of these reports pertain to living children with neurological abnormalities. CASE PRESENTATION: We report the case of a 14-month-old girl who was brought for treatment of unusual facies, growth retardation, and patent ductus arteriosus. Karyotype analysis revealed a 47, XX, + 10/46, XX pattern. MRI showed characteristics of Dandy-Walker syndrome and ventricular enlargement in the brain.

conclusionsThis case is distinguished by its extreme rarity and its potential for use as a reference case of this condition in clinical settings.

Indexed as

Abnormalities, MultipleDandy-Walker SyndromeMosaicismTrisomyUniparental DisomyBrainChromosomes, Human, Pair 10Ductus Arteriosus, PatentEchocardiographyFemaleForamen Ovale, PatentHumansInfantKaryotypingDandy–Walker syndromeMosaicism trisomy 10Nervous systemPatent ductus arteriosus

Identifiers

PMID30081864
PMCPMC6090700
OpenAlexW2886155378

What OpenQuestion holds

Textmetadata
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.