Cargando…

Should Prenatal Chromosomal Microarray Analysis Be Offered for Pulmonary Atresia? A Single-Center Retrospective Study in China

(1) Objective: To evaluate the application of chromosomal microarray analysis (CMA) in fetuses with pulmonary atresia (PA) and to explore the risk factors for predicting chromosomal imbalances and adverse perinatal outcomes. (2) Methods: This study investigated 428 cases of PA singleton pregnancies...

Descripción completa

Detalles Bibliográficos
Autores principales:	Wang, You, Ma, Chunling, Fu, Fang, Zhou, Hang, Cheng, Ken, Huang, Ruibin, Li, Ru, Li, Dongzhi, Liao, Can
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2023
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10047995/ https://www.ncbi.nlm.nih.gov/pubmed/36980994 http://dx.doi.org/10.3390/genes14030722

Ejemplares similares

Should prenatal chromosomal microarray analysis be offered for isolated ventricular septal defect? A single-center retrospective study from China
por: Cheng, Ken, et al.
Publicado: (2022)

Prenatal Diagnosis of Talipes Equinovarus by Ultrasound and Chromosomal Microarray Analysis: A Chinese Single-Center Retrospective Study
por: Huang, Ruibin, et al.
Publicado: (2022)

Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysis
por: Huang, Ruibin, et al.
Publicado: (2022)

Chromosome Microarray Analysis and Exome Sequencing: Implementation in Prenatal Diagnosis of Fetuses with Digestive System Malformations
por: Wang, You, et al.
Publicado: (2023)

Prenatal Diagnosis of Chromosome 16p11.2 Microdeletion
por: Wang, You, et al.
Publicado: (2022)

Prenatal diagnosis and perinatal outcomes of twin pregnancies disharmonious for one fetus with nuchal translucency above the 95th percentile
por: Wang, You, et al.
Publicado: (2023)

Prenatal Diagnosis and Outcomes in Fetuses with Hemivertebra
por: Zhou, Hang, et al.
Publicado: (2022)

Chromosomal microarray analysis in the prenatal diagnosis of orofacial clefts: Experience from a single medical center in mainland China
por: Jin, Han, et al.
Publicado: (2018)

Genetic diagnosis of fetal microcephaly at a single tertiary center in China
por: Wang, You, et al.
Publicado: (2023)

Should prenatal care providers offer pregnancy options counseling?
por: Berglas, Nancy F., et al.
Publicado: (2018)

Prenatal diagnosis of chromosomal aberrations by chromosomal microarray analysis in foetuses with ventriculomegaly
por: Wang, Jiamin, et al.
Publicado: (2020)

Application of chromosome microarray analysis in prenatal diagnosis
por: Xia, Mingjing, et al.
Publicado: (2020)

Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencing
por: Fu, Fang, et al.
Publicado: (2022)

Chromosomal mosaicism detected by karyotyping and chromosomal microarray analysis in prenatal diagnosis
por: Zhang, Yi, et al.
Publicado: (2020)

The difference between karyotype analysis and chromosome microarray for mosaicism of aneuploid chromosomes in prenatal diagnosis
por: Hao, MengZhe, et al.
Publicado: (2020)

Potentials and challenges of chromosomal microarray analysis in prenatal diagnosis
por: Liu, Xijing, et al.
Publicado: (2022)

Chromosome microarray analysis in the investigation of children with congenital heart disease
por: Wu, Xiao-li, et al.
Publicado: (2017)

Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis
por: Armengol, Lluís, et al.
Publicado: (2011)

Chromosomal Microarrays in Prenatal Diagnosis: Time for a Change of Policy?
por: Miny, Peter, et al.
Publicado: (2013)

Exome sequencing improves genetic diagnosis of congenital orofacial clefts
por: Yan, Shujuan, et al.
Publicado: (2023)

Detection of submicroscopic chromosomal aberrations by chromosomal microarray analysis for the prenatal diagnosis of central nervous system abnormalities
por: Song, Tingting, et al.
Publicado: (2020)

Prenatal chromosomal microarray analysis in foetuses with isolated absent or hypoplastic nasal bone
por: Shi, Xiaomei, et al.
Publicado: (2022)

Prenatal diagnosis and early childhood outcome of fetuses with extremely large nuchal translucency
por: Zhou, Hang, et al.
Publicado: (2023)

Effectiveness of Chromosomal Microarray Analysis for Prenatal Diagnosis of Fetal Echogenic Intracardiac Focus: A Single-Center Experience
por: Huang, Hailong, et al.
Publicado: (2021)

Prenatal Diagnosis Using Chromosomal Microarray Analysis in High-Risk Pregnancies
por: Hsiao, Ching-Hua, et al.
Publicado: (2022)

Induction of labour should be offered to all women at term: FOR: Induction of labour should be offered at term
por: Lightly, Kate, et al.
Publicado: (2019)

Prenatal diagnosis and molecular cytogenetic identification of small supernumerary marker chromosomes: analysis of three prenatal cases using chromosome microarray analysis
por: Xue, Huili, et al.
Publicado: (2020)

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

Fetal congenital gastrointestinal obstruction: prenatal diagnosis of chromosome microarray analysis and pregnancy outcomes
por: Ni, Mengyao, et al.
Publicado: (2023)

Application of Chromosomal Microarray and Multiplex Ligation-dependent Probe Amplification in prenatal diagnosis
por: Sharma, Pankaj, et al.
Publicado: (2014)

Prenatal genetic diagnosis of omphalocele by karyotyping, chromosomal microarray analysis and exome sequencing
por: Shi, Xiaomei, et al.
Publicado: (2021)

Prenatal Chromosomal Microarray Analysis: Does Increased Resolution Equal Increased Yield?
por: Mitrakos, Anastasios, et al.
Publicado: (2023)

Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysis
por: Xie, Xiaorui, et al.
Publicado: (2023)

Prenatal ultrasound diagnosis of cystic biliary atresia
por: Morel, Baptiste, et al.
Publicado: (2015)

Diagnostic accuracy and value of chromosomal microarray analysis for chromosomal abnormalities in prenatal detection: A prospective clinical study
por: Huang, Hailong, et al.
Publicado: (2021)

Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis
por: Wang, Huilin, et al.
Publicado: (2019)

Chromosomal microarray analysis versus noninvasive prenatal testing in fetuses with increased nuchal translucency
por: Wang, Chaohong, et al.
Publicado: (2022)

Prenatal diagnosis of fetuses conceived by assisted reproductive technology by karyotyping and chromosomal microarray analysis
por: Guo, Huan, et al.
Publicado: (2023)

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

Microarray Technology for the Diagnosis of Fetal Chromosomal Aberrations: Which Platform Should We Use?
por: Karampetsou, Evangelia, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_ml5qmj3bnl20ucobekb5lp8ff1