Evidence map›Paper›PMID 35601121›Full record

ArticleJGH open : an open access journal of gastroenterology and hepatology2022

Family with Peutz-Jeghers syndrome in Indonesia.

Muhammad Luthfi Parewangi, Resha Dermawansyah Rusman, Fardah Akil, Nu'man A S Daud, Rini Bachtiar, Susanto Hendra Kusuma, Amelia Rifai, Akiko Syawalidhany Tahir, Upik Miskad, Erwin Syarifuddin

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

Article in JGH open : an open access journal of gastroenterology and hepatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 95% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 1 institution in 1 country.

Muhammad Luthfi ParewangiDivision of Gastroenterology-Hepatology, Department of Internal Medicine, Faculty of Medicine Hasanuddin University Makassar Indonesia.ORCID https://orcid.org/0000-0001-9257-9344
Resha Dermawansyah RusmanDepartment of Internal Medicine, Faculty of Medicine Hasanuddin University Makassar Indonesia.ORCID https://orcid.org/0000-0002-2183-6611
Fardah AkilDivision of Gastroenterology-Hepatology, Department of Internal Medicine, Faculty of Medicine Hasanuddin University Makassar Indonesia.ORCID https://orcid.org/0000-0002-4222-6011
Nu'man A S DaudDivision of Gastroenterology-Hepatology, Department of Internal Medicine, Faculty of Medicine Hasanuddin University Makassar Indonesia.ORCID https://orcid.org/0000-0003-0931-0550
Rini BachtiarDivision of Gastroenterology-Hepatology, Department of Internal Medicine, Faculty of Medicine Hasanuddin University Makassar Indonesia.
Susanto Hendra KusumaDivision of Gastroenterology-Hepatology, Department of Internal Medicine, Faculty of Medicine Hasanuddin University Makassar Indonesia.
Amelia RifaiDivision of Gastroenterology-Hepatology, Department of Internal Medicine, Faculty of Medicine Hasanuddin University Makassar Indonesia.
Akiko Syawalidhany TahirDepartment of Internal Medicine, Faculty of Medicine Hasanuddin University Makassar Indonesia.ORCID https://orcid.org/0000-0001-9476-4463
Upik MiskadDepartment of Pathology Anatomy, Faculty of Medicine Hasanuddin University Makassar Indonesia.
Erwin SyarifuddinDivision of Digestive, Department of Surgery, Faculty of Medicine Hasanuddin University Makassar Indonesia.
Hasanuddin University · ID

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterised by mucocutaneous pigmentation, gastrointestinal polyps and an increased risk of gastrointestinal and other cancers. We report an Indonesian woman, aged 28, with black spots on her lips who had multiple polyps extending from the stomach to the rectum. Her father and a son also had mucocutaneous lesions but they did not undergo gastrointestinal investigations. All three had mutations in the serine/threonine kinase 11 gene (

Indexed as

autosomal dominant disordercancer riskPeutz–Jeghers syndrome

Identifiers

PMID35601121
PMCPMC9120882
OpenAlexW4223911310

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.