Evidence map›Paper›PMID 28096981›Full record

ArticleClinical case reports2017

Experience of Mowat-Wilson syndrome prenatal diagnosis for a Chinese family.

Qian Jiang, Xiaoxiao Zhang, Yinan Ma, Qi Li, Chunhua Zheng, Yuchun Yan, Zhen Zhang, Ping Xiao, Lin Su, Wei Cheng and 2 more

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Clinical case reports, 2017. 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
–field-weighted citation impact
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.

  1. Three NovelFrontiers in genetics · 2022
    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

12 authors.

Qian JiangDepartment of Medical Genetics Beijing Municipal Key Laboratory of Child Development and Nutriomics Capital Institute of Pediatrics Beijing China.
Xiaoxiao ZhangDepartment of Obstetric and Gynecology Peking University First Hospital Beijing China.
Yinan MaDepartment of Central Laboratory Peking University First Hospital Beijing China.
Qi LiDepartment of General Surgery Capital Institute of Pediatrics Beijing China.
Chunhua ZhengDepartment of Pediatric Heart Capital Institute of Pediatrics Affiliated Children's Hospital Beijing China.
Yuchun YanDepartment of Radiology Capital Institute of Pediatrics Affiliated Children's Hospital Beijing China.
Zhen ZhangDepartment of General Surgery Capital Institute of Pediatrics Beijing China.
Ping XiaoDepartment of Pathology Capital Institute of Pediatrics Affiliated Children's Hospital Beijing China.
Lin SuReproductive Medicine Center Clinical College of PLA Affiliated Anhui Medical University Hefei China.
Wei ChengDepartment of Surgery Beijing United Family Hospital Beijing China; Department of Pediatrics and Surgery Faculty of Medicine, Nursing and Health Sciences Monash University Melbourne Victoria Australia.
Hong PanDepartment of Central Laboratory Peking University First Hospital Beijing China.
Long LiDepartment of General Surgery Capital Institute of Pediatrics Beijing China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mowat-Wilson syndrome (MWS) is a complex developmental disorder. We report the first prenatal diagnosis provided for a family in mainland China after identifying the causal mutation for the proband. Special focus on MWS-related organs during prenatal ultrasound scan is described which is extremely important for genetic counseling of parents.

Indexed as

Causal mutationMowat–Wilson syndromeprenatal diagnosisZEB2

Identifiers

PMID28096981
PMCPMC5224777

What OpenQuestion holds

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Registered trials

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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.