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

Agenesis of the Ductus Venosus and Its Association With Genetic Abnormalities

3 Oct 2024

Abstract excerpt

OBJECTIVE: To investigate the association of agenesis of the ductus venosus (ADV) with genetic abnormalities using genetic studies-Chromosomal Microarray Analysis (CMA) and Exome Sequencing (ES). DESIGN: Retrospective study of all fetuses diagnosed with ADV between January 2013 and December 2022 in a tertiary center. RESULTS: ADV was diagnosed in 33 fetuses. The diagnosis was made at a mean gestational age of...

Read the complete abstract on PubMed

Topics

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

Share to Congenital heart defects research
Share to Fetal and Pediatric Neurological Disorders
Share to Gynecological conditions and treatments

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 39363392
DOI: 10.1002/pd.6678

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Agenesis of the Ductus Venosus and Its Association With Genetic AbnormalitiesPMID 39363392Read ↗

Prenatal features, associated co-morbidities and clinical course of agenesis of the ductus venosus in the current era.Semantic proximity Read ↗

Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis.Semantic proximity Read ↗

Prenatal Deep Phenotyping in Genetic Syndromes Diagnosed in the First Trimester of Pregnancy.Semantic proximity Read ↗

Pregnancy Outcomes and Genetic Etiology in Fetuses with Congenital Renal Agenesis: A Follow-up StudySemantic proximity Read ↗

Prenatally diagnosed chromosome 1p36 deletions: a retrospective case series, literature review, and genotype-phenotype correlations.Semantic proximity Read ↗

Prenatal Genetic Analysis of Fetal 17q12 Microdeletion Syndrome and Relation to Kidney AbnormalitiesSemantic proximity Read ↗

Genetic analysis and pregnancy outcomes of fetuses with kidney and urinary tract anomaliesSemantic proximity Read ↗

16p13.11 microdeletion/microduplication in fetuses: investigation of associated ultrasound phenotypes, genetic anomalies, and pregnancy outcome follow-upSemantic proximity Read ↗

Integrated Prenatal Genetic Evaluation of Renal Agenesis: Chromosomal Microarray Analysis, Whole Exome Sequencing, and Outcome Correlations in 203 Fetuses.Semantic proximity Read ↗

Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomalies.Semantic proximity Read ↗

Chromosomal Abnormality in Fetuses with Isolated Antenatal Hydronephrosis: Update for Prenatal Diagnosis and Genetic CounselingSemantic proximity Read ↗

Genetic etiology analysis of 73 fetuses with ventriculomegalySemantic proximity Read ↗

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