Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Clinical Guidelines for Diagnosis and Management of Juvenile Polyposis Syndrome in Children and Adults-Secondary Publication

24 Apr 2023

Abstract excerpt

Juvenile polyposis syndrome (JPS) is a rare disease characterized by multiple hamartomatous polyps within the gastrointestinal tract. SMAD4 or BMPR1A is known as a causative gene of JPS. Approximately 75% of newly diagnosed cases have an autosomal-dominantly inherited condition, whereas 25% are sporadic without previous history of polyposis in the family pedigree. Some patients with JPS develop gastrointestinal...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Gastric Cancer Management and Outcomes
Share to Gastrointestinal Tumor Research and Treatment
Share to Genetic factors in colorectal cancer

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 37113581
DOI: 10.23922/jarc.2023-002

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical Guidelines for Diagnosis and Management of Juvenile Polyposis Syndrome in Children and Adults-Secondary PublicationPMID 37113581Read ↗

Juvenile polyposis syndrome: An overviewSemantic proximity Read ↗

A review of juvenile polyposis syndrome.Semantic proximity Read ↗

Hamartomatous polyposis syndromes.Semantic proximity Read ↗

Pediatric juvenile polyposis syndromes: an update.Semantic proximity Read ↗

SMAD4 juvenile polyposis syndrome and hereditary haemorrhagic telangiectasia presenting in a middle-aged man as a large fungating gastric mass, polyposis in both upper and lower GI tract and iron deficiency anaemia, with no known family history.Semantic proximity Read ↗

Hamartomatous polyps - a clinical and molecular genetic study.Semantic proximity Read ↗

Juvenile polyposis syndromeSemantic proximity Read ↗

Hamartomatous polyps: Diagnosis, surveillance, and managementSemantic proximity Read ↗

Disease expression in juvenile polyposis syndrome: a retrospective survey on a cohort of 221 European patients and comparison with a literature-derived cohort of 473 SMAD4/BMPR1A pathogenic variant carriersSemantic proximity Read ↗

Appreciating the broad clinical features of SMAD4 mutation carriers: a multicenter chart review.Semantic proximity Read ↗

Juvenile polyposis syndrome in children: The impact of SMAD4 and BMPR1A mutations on clinical phenotype and polyp burden.Semantic proximity Read ↗

Juvenile polyposis syndrome: a study of genotype, phenotype, and long-term outcome.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.