Prenatally and postnatally sequential genetic etiology detection in corpus callosum abnormalities

Prenatally and postnatally sequential genetic etiology detection in corpus callosum abnormalities

Abstract To evaluate the clinical utility of genetic testing via karyotyping, chromosomal microarray analysis (CMA), and exome sequencing in cases with corpus callosum abnormalities (CCA). Here, 65 prenatal and 12 postnatal cases diagnosed with CCA via ultrasound and magnetic resonance imaging exami...

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Bibliographic Details
Main Authors: Huili Xue, Aili Yu, Lin Zheng, Xianglan Ye, Lin Zhang, Qun Guo, Lingji Chen, Qingmei Shen, Na lin, Hailong Huang, Liangpu Xu
Format: Article
Language:English
Published: Nature Portfolio 2025-07-01
Series:Scientific Reports
Subjects:
Corpus callosum abnormality
Agenesis of the corpus callosum
Whole exome sequencing
Magnetic resonance imaging
Cytogenetics
Online Access:https://doi.org/10.1038/s41598-025-07105-3
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https://doi.org/10.1038/s41598-025-07105-3

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