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

Prenatal diagnosis of maternal uniparental disomy 5 by amniocentesis associated with confined placental mosaicism for trisomy 5 and fetal trisomy 21 in a pregnancy.

Taiwanese journal of obstetrics & gynecology - 1 Nov 2020

Chen Chih-Ping, Chern Schu-Rern, Wang Liang-Kai, Wu Peih-Shan, Wu Fang-Tzu, Chen Yun-Yi, Town Dai-Dyi, Pan Chen-Wen, Wang Wayseen

Abstract excerpt

OBJECTIVE: We present prenatal diagnosis of maternal uniparental disomy (UPD) 5 by amniocentesis associated with confined placental mosaicism (CPM) for trisomy 5 and fetal trisomy 21 in a pregnancy. CASE REPORT: A 45-year-old woman underwent chorionic villus sampling (CVS) at 11 weeks of gestation because of maternal advanced age and an increased nuchal translucency of 4.0 mm in the first-trimester screening. CVS...

Read the complete abstract on PubMed

Topics

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

Share to Amniocentesis
Share to Chorionic Villi Sampling

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cytogenetic Analysis

Share to Down Syndrome

Share to Karyotype

Share to Live Birth

Share to Trisomy

Share to Uniparental Disomy

Source

Identifiers

PMID: 33218416
DOI: 10.1016/j.tjog.2020.09.023

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prenatal diagnosis of maternal uniparental disomy 5 by amniocentesis associated with confined placental mosaicism for trisomy 5 and fetal trisomy 21 in a pregnancy.PMID 33218416Read ↗

A prenatal diagnosis of mosaic trisomy 5 reveals a postnatal complete uniparental disomy of chromosome 5 with multiple congenital anomaliesSemantic proximity Read ↗

Prenatal diagnosis of low-level mosaicism for trisomy 21 by amniocentesis in a pregnancy associated with maternal uniparental disomy of chromosome 21 in the fetus and a favorable outcomeSemantic proximity Read ↗

Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphismSemantic proximity Read ↗

Prenatal testing for uniparental disomy: indications and clinical relevance.Semantic proximity Read ↗

Genome-wide detection of uniparental disomy in a fetus with intrauterine growth restriction using genotyping microarrays.Semantic proximity Read ↗

Low-level mosaic trisomy 9 at amniocentesis associated with a positive non-invasive prenatal testing for trisomy 9, maternal uniparental disomy 9, intrauterine growth restriction and a favorable fetal outcome in a pregnancySemantic proximity Read ↗

Prenatal diagnosis of maternal uniparental disomy 21 in association with low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with intrauterine growth restriction and a favorable outcomeSemantic proximity Read ↗

Prenatally detected trisomy 20 mosaicismSemantic proximity Read ↗

Prenatal diagnosis of mosaic trisomy 8: Clinical report and literature reviewSemantic proximity Read ↗

Rapid diagnosis of pseudomosaicism in a case of Level II mosaicism for trisomy 5 in a single colony from an in situ culture of amniocytes and a review of mosaic trisomy 5 at amniocentesisSemantic proximity Read ↗

Severe intrauterine growth restriction and trisomy 15 confined placental mosaicism: a case report and review of literatureSemantic proximity Read ↗

Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature reviewSemantic proximity Read ↗

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