Evidence map›Paper›PMID 33569485›Full record

ArticleAnnals of translational medicine2021

Prenatal diagnosis of harlequin ichthyosis by ultrasonography: a case report.

Xiao-Jing Zhou, Yu-Jie Lin, Xi-Wei Chen, Jia-Hua Zheng, Ying-Jie Zhou

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

Article in Annals of translational medicine, 2021. 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
0.8field-weighted citation impact, top 35% 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, 8 citations in OpenAlex.

  1. Article
  2. Review
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

5 authors at 3 institutions in 1 country.

Xiao-Jing ZhouSeven Section of Department of Gynaecology, the Second Hospital of Hebei Medical University, Shijiazhuang, China.
Yu-Jie LinDepartment of Ultrasound, the Julu County Hospital, Xingtai, China.
Xi-Wei ChenSeven Section of Department of Gynaecology, the Second Hospital of Hebei Medical University, Shijiazhuang, China.
Jia-Hua ZhengDepartment of Obstetrics and Gynecology, the Second Hospital of Hebei Medical University, Shijiazhuang, China.
Ying-Jie ZhouSeven Section of Department of Gynaecology, the Second Hospital of Hebei Medical University, Shijiazhuang, China.
Second Hospital of Hebei Medical University · CNHebei Medical University · CNXingtai People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autosomal recessive congenital ichthyosis is a genetically and phenotypically heterogeneous group of skin disorders, including harlequin ichthyosis (HI), lamellar ichthyosis, and bullous congenital ichthyosiform erythroderma. HI is the most phenotypically severe autosomal recessive congenital ichthyosis associated with the mutation of the adenosine triphosphate-binding cassette subfamily A member 12 (

Indexed as

case reportHarlequin ichthyosismolecular diagnosisprenatal diagnosisprenatal ultrasound

Identifiers

PMID33569485
PMCPMC7867921
OpenAlexW3123010017

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.