Evidence map›Paper›PMID 34189096›Full record

ArticleTranslational pediatrics2021

Case report of juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome: first report in Korea with a novel mutation in the

Ben Kang, Su-Kyeong Hwang, Sujin Choi, Eun Soo Kim, Sang Yub Lee, Chang-Seok Ki, Eun-Hae Cho, Ji-Hyuk Lee, Byung-Ho Choe

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

Article in Translational pediatrics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. A Case of Gastric Juvenile-Type Polyposis With SMAD4 Mutation.The Korean journal of helicobacter and upper gastrointestinal research · 2026
    Article
  2. Review
  3. Review
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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

9 authors at 3 institutions in 1 country.

Ben KangDepartment of Pediatrics, School of Medicine, Kyungpook National University, Daegu, South Korea.
Su-Kyeong HwangDepartment of Pediatrics, School of Medicine, Kyungpook National University, Daegu, South Korea.
Sujin ChoiDepartment of Pediatrics, School of Medicine, Kyungpook National University, Daegu, South Korea.
Eun Soo KimDepartment of Internal Medicine, School of Medicine, Kyungpook National University, Daegu, South Korea.
Sang Yub LeeDepartment of Radiology, School of Medicine, Kyungpook National University, Daegu, South Korea.
Chang-Seok KiGC Genome, Yongin, South Korea.
Eun-Hae ChoGC Genome, Yongin, South Korea.
Ji-Hyuk LeeDepartment of Pediatrics, Chungbuk National University College of Medicine, Cheongju, South Korea.
Byung-Ho ChoeDepartment of Pediatrics, School of Medicine, Kyungpook National University, Daegu, South Korea.
Kyungpook National University · KRGenome and Company (South Korea) · KRChungbuk National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Juvenile polyposis/hereditary hemorrhagic telangiectasia (JPS/HHT) syndrome is a rare, autosomal dominant disorder caused by mutations in the

Indexed as

arteriovenous malformation (AVM)childhereditary hemorrhagic telangiectasia (HHT)Juvenile polyposis syndrome (JPS)SMAD4

Identifiers

PMID34189096
PMCPMC8193005
OpenAlexW3155550217

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.