ArticleArchives of medical science : AMS2014
Juvenile polyposis syndrome.
Article in Archives of medical science : AMS, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.
What it found
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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.
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Who cites it
20 citing papers in PubMed, 39 citations in OpenAlex.
- Next-Generation Sequencing Panel Analysis of Clinically Relevant Mutations in Circulating Cell-Free DNA from Patients with Gestational Trophoblastic Neoplasia: A Pilot Study.BioMed research international · 2020Trial
- Review
- Identification of a MosaicCase reports in genetics · 2025Article
- Juvenile polyposis syndrome in a child with von Willebrand disease: a case report and literature review.Frontiers in pediatrics · 2025Article
- Pediatric Cancer Screening in Hereditary Gastrointestinal Cancer Risk Syndromes: An Update from the AACR Childhood Cancer Predisposition Working Group.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024Article
- Exploring Familial Adenomatous Polyposis Through Radiology: A Case Series and Literature Review.Cureus · 2024Article
- SMAD4 variants and its genotype-phenotype correlations to juvenile polyposis syndrome.Hereditary cancer in clinical practice · 2023Review
- Can aura migraine be elicited by isolated pulmonary arteriovenous fistula?-A case report.Frontiers in neurology · 2022Article
- mTOR inhibitors reduce enteropathy, intestinal bleeding and colectomy rate in patients with juvenile polyposis of infancy with PTEN-BMPR1A deletion.Human molecular genetics · 2021Article
- Phenotypic Differences in Juvenile Polyposis Syndrome With or Without a Disease-causingCancer prevention research (Philadelphia, Pa.) · 2021Article
- Juvenile polyposis syndrome might be misdiagnosed as familial adenomatous polyposis: a case report and literature review.BMC gastroenterology · 2020Review
- Gastrointestinal Polyposis in Pediatric Patients.Journal of pediatric gastroenterology and nutrition · 2019Review
- BMPR1A mutation-positive juvenile polyposis syndrome and atrial septal defect: coincidence or association?BMJ case reports · 2019Article
- Current Approaches to Pediatric Polyposis Syndromes.Clinics in colon and rectal surgery · 2018Review
- Hamartomatous Polyps and Associated Syndromes.Clinics in colon and rectal surgery · 2016Review
- Polyp Genetics.Clinics in colon and rectal surgery · 2016Review
- Molecular approach to genetic and epigenetic pathogenesis of early-onset colorectal cancer.World journal of gastrointestinal oncology · 2016Review
- Magnifying chromoendoscopic and endocytoscopic findings of juvenile polyps in the colon and rectum.Oncology letters · 2016Article
- Review
- Colorectal cancer risk in hamartomatous polyposis syndromes.World journal of gastrointestinal surgery · 2015Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Juvenile polyposis syndrome (JPS) is an autosomal dominant predisposition to the occurrence of hamartomatous polyps in the gastrointestinal tract. Diagnosis of JPS is based on the occurrence of numerous colon and rectum polyps or any number of polyps with family history and, in the case of juvenile polyps, their occurrence also outside the large intestine. The JPS is caused by mutations in SMAD4 and BMPR1A. Products of the SMAD4 gene are involved in signal transduction in the transforming growth factor β pathway and BMPR1A protein is a receptor belonging to the family of transmembrane serine/threonine kinases. Both proteins are responsible for processes determining appropriate development of colonic mucosa. The JPS belongs to the group of hamartomatous polyposes. The hamartomatous polyposis syndromes constitute a group of diseases in which manifestations differ slightly and only molecular diagnostics gives the possibility of verifying the clinical diagnosis.
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What OpenQuestion holds
Registered trials
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.