ReviewChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2020
Prenatal genetic considerations in congenital ventriculomegaly and hydrocephalus.
Review in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.
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Who cites it
24 citing papers in PubMed, 48 citations in OpenAlex.
- Dangling Choroid Plexus: An Early Sign of Fetal Anomaly.Diagnostics (Basel, Switzerland) · 2026Article
- Pregnancy and early neurodevelopment after prenatal ventriculomegaly: a 2011-2024 single-center retrospective cohort of 983 cases.BMC pregnancy and childbirth · 2026Article
- Clinical characteristics and outcome of fetuses with ventriculomegaly: a retrospective multicenter study.Archives of gynecology and obstetrics · 2026Article
- Neonatal encephalopathy and hypoxic-ischemic encephalopathy: the state of the art.Pediatric research · 2025Review
- De novo variants disrupt an LDB1-regulated transcriptional network in congenital ventriculomegaly.Brain : a journal of neurology · 2025Article
- Fetal Corpus Callosum Anomalies: A Review of Underlying Genetic Disorders and Prenatal Testing Options.Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine · 2025Review
- Case Report: Ultralow-field portable MRI improves the diagnosis of congenital hydrocephalus.Frontiers in pediatrics · 2025Article
- Current Diagnostic, Counseling, and Treatment Options in Non-Severe and Severe Apparently Isolated Fetal Ventriculomegaly.Biomedicines · 2024Review
- TRIM71 mutations cause a neurodevelopmental syndrome featuring ventriculomegaly and hydrocephalus.Brain : a journal of neurology · 2024Article
- Clinical characteristics and perinatal outcome of fetuses with ventriculomegaly.Archives of gynecology and obstetrics · 2024Article
- Two Novel Variants Associated with Brain Abnormalities in Clinical Suspicion of Arthrogryposis and Similar Phenotype in Three Children: Challenges in Offering Prenatal Diagnosis.Journal of obstetrics and gynaecology of India · 2024Article
- A novel SMARCC1 BAFopathy implicates neural progenitor epigenetic dysregulation in human hydrocephalus.Brain : a journal of neurology · 2024Article
- Genetic and molecular mechanisms of hydrocephalus.Frontiers in molecular neuroscience · 2024Review
- Fetal brain MRI: neurometrics, typical diagnoses, and resolving common dilemmas.The British journal of radiology · 2023Review
- White matter changes in fetal brains with ventriculomegaly.Frontiers in neuroanatomy · 2023Article
- Fetal cerebral ventriculomegaly: What do we tell the prospective parents?Prenatal diagnosis · 2022Review
- [Pregnancy Outcomes and Prognosis of Fetal Ventriculomegaly: A Retrospective Cohort Study].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2022Article
- CNS Malformations in the Newborn.Maternal health, neonatology and perinatology · 2022Review
- Risk Assessment of the Increased Occurrence of Congenital Cardiac and Non-Cardiac Defects in Fetuses with a Normal Karyotype after Assisted Fertilization in Comparison to Natural Fertilization Based on Ultrasound Diagnostics.Journal of clinical medicine · 2021Article
- Genomics of human congenital hydrocephalus.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021Article
Corrections and comments
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Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundFetal ventriculomegaly (VM) is a frequent finding in prenatal ultrasound. Rather than a proper diagnosis, VM is a sonographic sign, making prenatal counseling a complex and challenging undertaking. VM can range from severe pathologic processes leading to severe neurodevelopmental delay to normal variants. DISCUSSION: A growing number of genetic conditions with different pathophysiological mechanisms, inheritance patterns, and long-term prognosis have been associated both to isolated and complex fetal VM. These include chromosomal abnormalities, copy number variants, and several single gene diseases. In this review, we describe some of the most common genetic conditions associated with fetal VM and provide a simplified diagnostic workflow for the clinician.
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