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Detection of copy number variation associated with ventriculomegaly in fetuses using single nucleotide polymorphism arrays.

Scientific reports - 5 Mar 2021

Xue Huili, Yu Aili, Lin Na, Chen Xuemei, Lin Min, Wang Yan, Huang Hailong, Xu Liangpu

Abstract excerpt

Etiopathogenesis of fetal ventriculomegaly is poorly understood. Associations between fetal isolated ventriculomegaly and copy number variations (CNVs) have been previously described. We investigated the correlations between fetal ventriculomegaly-with or without other ultrasound anomalies-and chromosome abnormalities. 222 fetuses were divided into four groups: (I) 103 (46.4%) cases with isolated...

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Abnormal Karyotype
DNA Copy Number Variations
Fetus
Gestational Age
Hydrocephalus

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Prenatal Diagnosis

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PMID: 33674646
DOI: 10.1038/s41598-021-83147-7
PMCID: PMC7935846

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