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

The placenta in Beckwith-Wiedemann syndrome: genotype-phenotype associations, excessive extravillous trophoblast and placental mesenchymal dysplasia.

Pathology - 1 Oct 2012

Armes Jane E, McGown Ivan, Williams Mark, Broomfield Amy, Gough Karen, Lehane Fiona, Lourie Rohan

Abstract excerpt

AIMS: Placental mesenchymal dysplasia (PMD) is a rare condition which is associated with the disparate fetal outcomes of Beckwith-Wiedemann syndrome (BWS), fetal growth restriction or intrauterine and neonatal death. We aimed to investigate the potential epigenetic/genetic anomalies associated with PMD and their relationship with the different causes of BWS. METHODS: Eight archival cases in which PMD, BWS or both...

Read the complete abstract on PubMed

Topics

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

Share to Beckwith-Wiedemann Syndrome
Share to Chromosomes, Human, Pair 11

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

Share to Cyclin-Dependent Kinase Inhibitor p57

Share to DNA Methylation

Share to Epigenomics

Share to Insulin-Like Growth Factor II

Share to Placenta

Share to Trophoblasts

Source

Identifiers

PMID: 22772341
DOI: 10.1097/PAT.0b013e3283559c94

Genes

IGF2

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

The placenta in Beckwith-Wiedemann syndrome: genotype-phenotype associations, excessive extravillous trophoblast and placental mesenchymal dysplasia.PMID 22772341Read ↗

Placental Mesenchymal Dysplasia and Beckwith–Wiedemann SyndromeSemantic proximity Read ↗

Aberrant hypomethylation at imprinted differentially methylated regions is involved in biparental placental mesenchymal dysplasiaSemantic proximity Read ↗

The clinical phenotype of mosaicism for genome-wide paternal uniparental disomy: two new reports.Semantic proximity Read ↗

Epimutation profiling in Beckwith-Wiedemann syndrome: relationship with assisted reproductive technologySemantic proximity Read ↗

Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders.Semantic proximity Read ↗

Placental Mesenchymal Dysplasia Is Associated With High Rates of Intrauterine Growth Restriction and Fetal DemiseSemantic proximity Read ↗

Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development.Semantic proximity Read ↗

Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjectsSemantic proximity Read ↗

Clinical and Molecular Diagnosis of Beckwith-Wiedemann Syndrome with Single- or Multi-Locus Imprinting Disturbance.Semantic proximity Read ↗

(Epi)genotype–phenotype correlations in Beckwith–Wiedemann syndrome: a paradigm for genomic medicineSemantic proximity Read ↗

Beckwith-Wiedemann syndrome and assisted reproduction technology (ART): Table 1Semantic proximity Read ↗

Placental Mesenchymal Dysplasia Is Associated With High Rates of Intrauterine Growth Restriction and Fetal Demise: A Report of 11 New Cases and a Review of the LiteratureSemantic proximity Read ↗

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