Evidence map›Paper›PMID 32528861›Full record

ArticleCase reports in women's health2020

Polyhydramnios and abnormal foetal heart rate patterns in a foetus with Prader-Willi syndrome: A case report.

Tsuyoshi Murata, Toma Fukuda, Aya Kanno, Hyo Kyozuka, Akiko Yamaguchi, Hiromi Shimizu, Takafumi Watanabe, Keiya Fujimori

Open access · goldAbstract readCase Reports
In one paragraph

Article in Case reports in women's health, 2020. 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
0.7field-weighted citation impact, top 26% 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, 6 citations in OpenAlex.

  1. Article
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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

8 authors at 1 institution in 1 country.

Tsuyoshi MurataDepartment of Obstetrics and Gynecology, Fukushima Medical University School of Medicine, Fukushima, Japan.
Toma FukudaDepartment of Obstetrics and Gynecology, Fukushima Medical University School of Medicine, Fukushima, Japan.
Aya KannoDepartment of Obstetrics and Gynecology, Fukushima Medical University School of Medicine, Fukushima, Japan.
Hyo KyozukaDepartment of Obstetrics and Gynecology, Fukushima Medical University School of Medicine, Fukushima, Japan.
Akiko YamaguchiDepartment of Obstetrics and Gynecology, Fukushima Medical University School of Medicine, Fukushima, Japan.
Hiromi ShimizuDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Takafumi WatanabeDepartment of Obstetrics and Gynecology, Fukushima Medical University School of Medicine, Fukushima, Japan.
Keiya FujimoriDepartment of Obstetrics and Gynecology, Fukushima Medical University School of Medicine, Fukushima, Japan.
Fukushima Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPrader-Willi syndrome (PWS) is a complex neurodevelopmental genetic disorder. No definitive clinical signs of antenatal PWS have been identified. CASE: A healthy, nulliparous, 29-year-old woman demonstrated polyhydramnios at 27 weeks of gestation. Cardiotocography (CTG) showed an absence of foetal heart rate (FHR) acceleration and moderate FHR variability. Daily CTG demonstrated an absence of FHR acceleration. A male newborn was delivered by caesarean section, weighing 2492 g, which is appropriate for gestational age; the Apgar scores at 1 and 5 min were 6 and 6, respectively, and the umbilical artery pH was 7.295. The newborn exhibited marked hypotonia, lack of sucking, and cryptorchidism. FISH analysis performed due to severe hypotonia showed 46, XY. Ish del (15) (q11. 2q 11.2), which led to the diagnosis of PWS. DISCUSSION: Polyhydramnios and abnormal FHR patterns may be associated with feeding difficulty and hypotonia. These signs may be an indication for antenatal molecular genetic testing to diagnose PWS.

Indexed as

Abnormal foetal heart rate patternsMolecular genetic testingPolyhydramniosPrader-Willi syndrome

Identifiers

PMID32528861
PMCPMC7283086
OpenAlexW3029928511

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.