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

Gardner's syndrome (familial adenomatous polyposis): a cilia-related disorder.

The Lancet. Oncology - 1 Jul 2009

Gómez García Encarna B, Knoers Nine V A M

Abstract excerpt

Familial adenomatous polyposis (FAP) is an autosomal dominant form of intestinal polyposis and colorectal cancer caused by germ-line mutations in the adenomatous polyposis coli (APC) gene. The term Gardner's syndrome is used to describe extracolonic manifestations, such as osteomas, skin cysts, congenital hypertrophy of the retinal pigmented epithelium (CHRPE), and desmoid tumours (aggressive fibromatosis), that...

Read the complete abstract on PubMed

Topics

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

Share to beta Catenin
Share to Ciliary Motility Disorders
Share to Genes, APC

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Genotype

Share to Microtubule-Associated Proteins

Share to Mutation

Share to Phenotype

Share to Signal Transduction

Source

Identifiers

PMID: 19573802
DOI: 10.1016/S1470-2045(09)70167-6

Genes

FAP
APC

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Gardner's syndrome (familial adenomatous polyposis): a cilia-related disorder.PMID 19573802Read ↗

Ocular manifestations of familial adenomatous polyposis (Gardner syndrome).Semantic proximity Read ↗

Gardner syndrome: skin manifestations, differential diagnosis and management.Semantic proximity Read ↗

Challenges in diagnosing and interdisciplinary treatment of a patient with Gardner syndrome: a case reportSemantic proximity Read ↗

[Rare hereditary syndromes associated with polyposis and the development of malignant tumors].Semantic proximity Read ↗

[Familial adenomatous polyposis syndrome (FAP): pathogenesis and molecular mechanisms].Semantic proximity Read ↗

Gardner syndrome in a Tunisian family: Identification of a rare APC mutation through targeted NGS.Semantic proximity Read ↗

Intestinal polyposis syndromes: progress in understanding and treatment.Semantic proximity Read ↗

Familial adenomatous polyposis (FAP): genotype correlation to FAP phenotype with osteomas and sebaceous cysts.Semantic proximity Read ↗

Peutz-Jeghers syndrome.Semantic proximity Read ↗

Novel Mutation in APC Gene Associated with Multiple Osteomas in a Family and Review of Genotype-Phenotype Correlations of Extracolonic Manifestations in Gardner SyndromeSemantic proximity Read ↗

Cilia, adenomatous polyposis coli and associated diseases.Semantic proximity Read ↗

APC gene mutations and extraintestinal phenotype of familial adenomatous polyposis.Semantic proximity Read ↗

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