Evidence map›Paper›PMID 38737280›Full record

ArticleHeliyon2024

Prenatal diagnosis of cleidocranial dysplasia: Case report on two cases with a negative family history.

Ruizheng Han, Chunshuang Zhang, Xiling Fu, Zhengfeng Zhu, Xinxia Wang, Hezhou Li

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

Article in Heliyon, 2024. 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. 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

6 authors.

Ruizheng HanDepartment of Diagnostic Ultrasound, the Third Affiliated Hospital of Zhengzhou University, Women and Children's Hospital of Henan Province, Health Center for Women and Children of Henan Province, Zhengzhou, Henan Province, China.
Chunshuang ZhangDepartment of Diagnostic Ultrasound, the Third Affiliated Hospital of Zhengzhou University, Women and Children's Hospital of Henan Province, Health Center for Women and Children of Henan Province, Zhengzhou, Henan Province, China.
Xiling FuDepartment of Diagnostic Ultrasound, the Third Affiliated Hospital of Zhengzhou University, Women and Children's Hospital of Henan Province, Health Center for Women and Children of Henan Province, Zhengzhou, Henan Province, China.
Zhengfeng ZhuDepartment of Diagnostic Ultrasound, the Third Affiliated Hospital of Zhengzhou University, Women and Children's Hospital of Henan Province, Health Center for Women and Children of Henan Province, Zhengzhou, Henan Province, China.
Xinxia WangDepartment of Diagnostic Ultrasound, the Third Affiliated Hospital of Zhengzhou University, Women and Children's Hospital of Henan Province, Health Center for Women and Children of Henan Province, Zhengzhou, Henan Province, China.
Hezhou LiDepartment of Diagnostic Ultrasound, the Third Affiliated Hospital of Zhengzhou University, Women and Children's Hospital of Henan Province, Health Center for Women and Children of Henan Province, Zhengzhou, Henan Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal dysplasia that presents with abnormalities in the craniofacial region, teeth, and clavicles and is linked to Case reports: Case 1 (a 26-year-old woman): ultrasound at 13 weeks showed a thickened nuchal translucency with absent nasal bones and poor ossifications in the cranium and vertebrae. Genetic testing confirmed a frame shift deletion of Conclusion: These cases underscore the importance of sonographic examination for prenatal CCD diagnosis with a negative family history. By reviewing previous cases, we concluded that combining NB hypoplasia, clavicle and skull hypoplasia, and shortened long bones may be effective for early screening for CCD. Prenatal diagnosis is crucial for guiding medical decisions.

Indexed as

Case reportCleidocranial dysplasiaNasal bone hypoplasiaPrenatal ultrasound

Identifiers

PMID38737280
PMCPMC11087947

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.