The application of chromosomal microarray analysis to the prenatal diagnosis of isolated mild ventriculomegaly

The application of chromosomal microarray analysis to the prenatal diagnosis of isolated mild ventriculomegaly

Objective: To investigate the clinical value of chromosomal microarray analysis (CMA) in the prenatal diagnosis of genetic abnormalities in fetal isolated mild ventriculomegaly. Materials and methods: This retrospective study reviewed 101 fetuses with isolated mild ventriculomegaly who had undergone...

Full description

Bibliographic Details
Main Authors:	Hong-Lei Duan, Xiang-Yu Zhu, Yu-Jie Zhu, Xing Wu, Guang-Feng Zhao, Wan-Jun Wang, Jie Li
Format:	Article
Language:	English
Published:	Elsevier 2019-03-01
Series:	Taiwanese Journal of Obstetrics & Gynecology
Online Access:	http://www.sciencedirect.com/science/article/pii/S1028455919300154

Similar Items

Evaluation of prenatal diagnosis of isolated ventriculomegaly
by: Teramoto Chika, et al.
Published: (2010-12-01)

Prenatal diagnosis of Smith–Magenis syndrome in two fetuses with increased nuchal translucency, mild lateral ventriculomegaly, and congenital heart defects
by: Ting-Ying Lei, et al.
Published: (2016-12-01)

Application of chromosome microarray analysis in prenatal diagnosis
by: Mingjing Xia, et al.
Published: (2020-11-01)

Asymmetric cortical development and prognosis in fetuses with isolated mild fetal ventriculomegaly: an observational prospective study
by: Rong Zhu, et al.
Published: (2021-03-01)

Role of foeral MRI in the diagnosis and prognosis of cerebral ventriculomegaly assessed by prenatal ultrasonography
by: Maria Inês Moreira Vieites Branco
Published: (2019)

Isolated ventriculomegaly: diagnosis, etiology and pre-natal management
by: Maria Inês Moreira Veiga Rodrigues
Published: (2021)

Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 1q42.3-q44 deletion in a fetus associated with ventriculomegaly on prenatal ultrasound
by: Chih-Ping Chen, et al.
Published: (2020-07-01)

The use of chromosomal microarray analysis in prenatal diagnosis of small supernumerary marker chromosome
by: Min-Hui Huang, et al.
Published: (2018)

Chromosomal Microarrays in Prenatal Diagnosis: Time for a Change of Policy?
by: Peter Miny, et al.
Published: (2013-12-01)

Second-trimester Molecular Prenatal Diagnosis of Sporadic Apert Syndrome Following Sonographic Findings of Mild Ventriculomegaly and Clenched Hands Mimicking Trisomy 18
by: Chih-Ping Chen, et al.
Published: (2010-03-01)

Prenatal diagnosis of mosaic trisomy 8 by amniocentesis in a fetus with ventriculomegaly and dysgenesis of the corpus callosum
by: Chih-Ping Chen, et al.
Published: (2020-01-01)

Prenatal diagnosis of a de novo 17p13.1 microduplication in a fetus with ventriculomegaly and lissencephaly
by: Chih-Ping Chen, et al.
Published: (2011-12-01)

Diagnostic Value of Magnetic Resonance Imaging in Fetal Lateral Ventriculomegaly and the Relationship Between the Degree of Isolated Lateral Ventriculomegaly and Neonatal Prognosis
by: Xiao-Min Zhao, et al.
Published: (2020-01-01)

Prenatal Diagnosis of Central Nervous System Anomalies by High-Resolution Chromosomal Microarray Analysis
by: Lijuan Sun, et al.
Published: (2015-01-01)

Prenatal Diagnosis of True Fetal Mosaicism with Small Supernumerary Marker Chromosome Derived from Chromosome 16 by Funipuncture and Molecular Cytogenetics Including Chromosome Microarray
by: Tien-Yu Yao, et al.
Published: (2021-08-01)

In utero MR for ventriculomegaly
by: Paley MNJ, et al.
Published: (2005-12-01)

Evaluation of fetal ventriculomegaly
by: Özgür Aydın, et al.
Published: (2013-06-01)

Cost-effectiveness analysis of chromosomal microarray as a primary test for prenatal diagnosis in Hong Kong
by: Claudia Ching Yan Chung, et al.
Published: (2020-02-01)

Repetitive Mild Traumatic Brain Injury Induces Ventriculomegaly and Cortical Thinning in Juvenile Rats
Published: (2014)

Cortical folding alterations in fetuses with isolated non-severe ventriculomegaly
by: Oualid M. Benkarim, et al.
Published: (2018-01-01)

Chromosomal microarray analysis in fetuses with high-risk prenatal indications: A retrospective study in China
by: Xiaomei Luo, et al.
Published: (2021-03-01)

Application of chromosomal microarray analysis in products of miscarriage
by: Xiangyu Zhu, et al.
Published: (2018-08-01)

Brain development in fetal ventriculomegaly
by: Kyriakopoulou, Vanesa
Published: (2013)

FETAL CEREBRAL “BORDERLINE” VENTRICULOMEGALY
by: Claudiu Marginean, et al.
Published: (2016-12-01)

Chromosomal Microarray Analysis for the Prenatal Diagnosis in Fetuses with Nasal Bone Hypoplasia: A Retrospective Cohort Study
by: Huang H, et al.
Published: (2021-04-01)

Outcome of 167 fetuses diagnosed <it>in utero </it>as having apparently isolated ventriculomegaly
by: Bannister C, et al.
Published: (2004-12-01)

Frequency and clinical manifestation of prenatal cytogenetic diagnosis of chromosomal polymorphisms in Northeast China
by: Li-Li Luo, et al.
Published: (2020-11-01)

Effectiveness of Chromosomal Microarray Analysis for Prenatal Diagnosis of Fetal Echogenic Intracardiac Focus: A Single-Center Experience
by: Huang H, et al.
Published: (2021-05-01)

Chromosomal microarray in isolated congenital and developmental cataract
by: Thales A. C De Guimarães, et al.
Published: (2021-01-01)

Altered white matter and cortical structure in neonates with antenatally diagnosed isolated ventriculomegaly
by: G. Lockwood Estrin, et al.
Published: (2016-01-01)

Prenatal Diagnostic Value of Chromosomal Microarray in Fetuses with Nuchal Translucency Greater than 2.5 mm
by: Zhu Zhang, et al.
Published: (2019-01-01)

Chromosome 1p32-p31 deletion syndrome: Prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction
by: Chih-Ping Chen, et al.
Published: (2011-09-01)

Submicroscopic aberrations of chromosome 16 in prenatal diagnosis
by: Xiaoqing Wu, et al.
Published: (2019-08-01)

Prenatal diagnosis of a fetus with mosaic ring chromosome 13: Case report and review of the literature
by: Xiao-Nan Hu, et al.
Published: (2021-05-01)

Second‐trimester prenatal diagnosis of Nager syndrome with a deletion including SF3B4 detected by chromosomal microarray
by: Malgorzata Drozniewska, et al.
Published: (2020-03-01)

Prenatal diagnosis of paternal uniparental disomy for chromosome 14 using a single-nucleotide-polymorphism-based microarray analysis: A case report
by: Chih-Ling Chen, et al.
Published: (2019-03-01)

Non-invasive prenatal diagnosis of chromosomal abnormalities by isolation of fetal cells from the maternal circulation
by: Al-Mufti, Raghad Abdul Wahab Mohamed Latif
Published: (2003)

Genetic counseling for a prenatal diagnosis of structural chromosomal abnormality with high-resolution analysis using a single nucleotide polymorphism microarray
by: Akiko Takashima, et al.
Published: (2016-08-01)

Prenatal Diagnosis of Monosomy 17p (17p 13.3 → pter) Associated With Polyhydramnios, Intrauterine Growth Restriction, Ventriculomegaly, and Miller-Dieker Lissencephaly Syndrome in a Fetus
by: Chin-Yi Lin, et al.
Published: (2009-12-01)

Evaluation of molecular tests for prenatal diagnosis of chromosome abnormalities
by: G.M. Grimshaw, et al.
Published: (2003-01-01)