Prenatal detection of chromosomal abnormalities and copy number variants in fetuses with ventriculomegaly.

CONCLUSIONS: CMA is highly recommended for prenatal diagnosis of fetal VM together with karyotyping, especially in fetuses with bilateral VM and NIVM with abnormal CNS findings. Further study is necessary to explore the relationships between genotypes and phenotypes to facilitate prenatal diagnosis of fetal VM.
PMID: 32014392 [PubMed - as supplied by publisher]

Source: European Journal of Paediatric Neurology - January 21, 2020 Category: Neurology Authors: Chang Q, Yang Y, Peng Y, Liu S, Li L, Deng X, Yang M, Lan Y Tags: Eur J Paediatr Neurol Source Type: research