ArticleGastroenterology & hepatology2010
Hereditary hamartomatous polyposis syndromes: understanding the disease risks as children reach adulthood.
Article in Gastroenterology & hepatology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.
What it found
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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.
The trial behind it
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Who cites it
23 citing papers in PubMed.
- The potential of oral healthcare providers to recognise early systemic disease.British dental journal · 2025Review
- Polyposis found on index colonoscopy in a 56-year-old female -World journal of gastrointestinal endoscopy · 2023Article
- Juvenile polyposis diagnosed with an integrated histological, immunohistochemical and molecular approach identifying new SMAD4 pathogenic variants.Familial cancer · 2022Article
- Unusual case of small bowel intussusception in adult revealing a Peutz-Jeghers syndrome.BJR case reports · 2022Article
- Importance of early detection of juvenile polyposis syndrome: A case report and literature review.Medicine · 2020Review
- Chromosomal translocation disrupting the SMAD4 gene resulting in the combined phenotype of Juvenile polyposis syndrome and Hereditary Hemorrhagic Telangiectasia.Molecular genetics & genomic medicine · 2020Article
- BMPR1A mutation-positive juvenile polyposis syndrome and atrial septal defect: coincidence or association?BMJ case reports · 2019Article
- A Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes.Journal of genetic counseling · 2017Review
- A rare case of synchronous colocolic intussusception in association with Peutz-Jeghers syndrome.BJR case reports · 2017Article
- The biological complexity of colorectal cancer: insights into biomarkers for early detection and personalized care.Therapeutic advances in gastroenterology · 2016Review
- Giant Adrenal Cavernous Hemangioma in a Patient with Familial Adenomatous Polyposis.Clinics and practice · 2016Article
- Hamartomatous Tumors in the Gastrointestinal Tract.Gastrointestinal tumors · 2015Review
- Genetics, diagnosis and management of colorectal cancer (Review).Oncology reports · 2015Review
- Overlap of Juvenile polyposis syndrome and Cowden syndrome due to de novo chromosome 10 deletion involving BMPR1A and PTEN: implications for treatment and surveillance.American journal of medical genetics. Part A · 2015Article
- Hamartomatous polyposis syndromes: a review.Orphanet journal of rare diseases · 2014Review
- Hamartomatous polyposis syndromes.Hereditary cancer in clinical practice · 2013Article
- Autosomal Dominant Inherited Cowden's Disease in a Family.Clinical endoscopy · 2013Article
- Differential expression of PTEN gene correlates with phenotypic heterogeneity in three cases of patients showing clinical manifestations of PTEN hamartoma tumour syndrome.Hereditary cancer in clinical practice · 2013Article
- Juvenile polyposis, hereditary hemorrhagic telangiectasia, and early onset colorectal cancer in patients with SMAD4 mutation.Journal of gastroenterology · 2012Article
- Beta catenin and cytokine pathway dysregulation in patients with manifestations of the "PTEN hamartoma tumor syndrome".BMC medical genetics · 2012Article
Corrections and comments
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Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Hamartomatous polyposis syndromes are a rare group of hereditary autosomal dominant disorders that comprise less than 1% of all hereditary colorectal cancers. Hamartomatous polyps, in and of themselves, are benign entities; however, these hamartomatous polyposis syndromes have a malignant potential for the development of colorectal cancer as well as extracolonic cancers. Early detection and proper surveillance are vital to minimizing the risk of carcinoma. This article provides a critical review of the clinical presentation, pathology, genetics, and screening and surveillance guidelines of juvenile polyposis syndrome, PTEN hamartoma tumor syndrome, and Peutz-Jeghers syndrome.
Indexed as
Identifiers
20567567PMC2886463What 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.