Evidence map›Paper›PMID 42670380›Full record

ArticleCase reports in surgery2026

Familial Juvenile Polyposis Syndrome: A Case Report of a Cosegregation of SMAD4 Germline Pathogenic Variant c.403C>T and Review of the Literature.

Carlos Augusto Real Martinez, Giovanna Savoy Pazin, Rayama Moreira Siqueira, Rita Barboza de Carvalho, Michel Gardere Camargo, Lívia Moreira Genaro, Pedro Henrique Leite Bonfitto, Maria de Lourdes Setsuko Ayrizono, Raquel Franco Leal, Cláudio Saddy Rodrigues Coy

Abstract read
In one paragraph

Article in Case reports in surgery, 2026. 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

10 authors.

Carlos Augusto Real MartinezColorectal Surgery Unit, Department of Surgery, Universidade Estadual de Campinas (UNICAMP), Campinas, São Paulo, Brazil, unicamp.br.ORCID https://orcid.org/0000-0001-8088-427X
Giovanna Savoy PazinColorectal Surgery Unit, Department of Surgery, Universidade Estadual de Campinas (UNICAMP), Campinas, São Paulo, Brazil, unicamp.br.ORCID https://orcid.org/0000-0001-6285-9636
Rayama Moreira SiqueiraPost-graduate Program in Surgical Sciences, School of Medical Sciences, University of Campinas (Unicamp), Campinas, São Paulo, Brazil, unicamp.br.ORCID https://orcid.org/0000-0001-7909-8810
Rita Barboza de CarvalhoPathology Division, Gastrocenter, University of Campinas (Unicamp), Campinas, São Paulo, Brazil, unicamp.br.
Michel Gardere CamargoColorectal Surgery Unit, Department of Surgery, Universidade Estadual de Campinas (UNICAMP), Campinas, São Paulo, Brazil, unicamp.br.ORCID https://orcid.org/0000-0001-6820-8164
Lívia Moreira GenaroColorectal Surgery Unit, Department of Surgery, Universidade Estadual de Campinas (UNICAMP), Campinas, São Paulo, Brazil, unicamp.br.ORCID https://orcid.org/0000-0002-4640-6554
Pedro Henrique Leite BonfittoColorectal Surgery Unit, Department of Surgery, Universidade Estadual de Campinas (UNICAMP), Campinas, São Paulo, Brazil, unicamp.br.ORCID https://orcid.org/0000-0003-4491-7737
Maria de Lourdes Setsuko AyrizonoColorectal Surgery Unit, Department of Surgery, Universidade Estadual de Campinas (UNICAMP), Campinas, São Paulo, Brazil, unicamp.br.ORCID https://orcid.org/0000-0002-7035-2568
Raquel Franco LealColorectal Surgery Unit, Department of Surgery, Universidade Estadual de Campinas (UNICAMP), Campinas, São Paulo, Brazil, unicamp.br.ORCID https://orcid.org/0000-0003-4285-4402
Cláudio Saddy Rodrigues CoyColorectal Surgery Unit, Department of Surgery, Universidade Estadual de Campinas (UNICAMP), Campinas, São Paulo, Brazil, unicamp.br.ORCID https://orcid.org/0000-0002-0916-4138

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Juvenile polyposis syndrome (JPS) is an inherited autosomal dominant disease that is distinguished by the emergence of numerous juvenile polyps within the gastrointestinal (GI) tract and has an increased risk of cancer. JPS is associated with germline mutations of the

Indexed as

case reportcolorectal neoplasmsintestinal polyposisjuvenile polyposis syndromeSMAD4 protein

Identifiers

PMID42670380
PMCPMC13526237

What OpenQuestion holds

Textmetadata
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.