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Article

Mucinous cystadenoma of ovary in a patient with juvenile polyposis due to 10q23 microdeletion: expansion of phenotype.

American journal of medical genetics. Part A - 1 Oct 2010

Babovic Nikola, Simmons Patricia S, Moir Christopher, Thorland Erik C, Scheithauer Bernd, Gliem Troy J, Babovic-Vuksanovic Dusica

Abstract excerpt

Juvenile polyposis syndrome (JPS) is a hereditary condition characterized by development of gastrointestinal polyps, and caused by mutations in SMAD4 or BMPR1A genes. Juvenile polyps can also be found in a related group of syndromes with multisystemic involvement including Cowden disease, Lhermit...

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Share to Adenomatous Polyposis Coli
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Share to Chromosomes, Human, Pair 10

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Comparative Genomic Hybridization

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Source

Identifiers

PMID: 20815035
DOI: 10.1002/ajmg.a.33637

Genes

PTEN
SMAD4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20815035-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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