Cargando…

Outcome after Prenatal Diagnosis of Trisomy 13, 18, and 21 in Fetuses with Congenital Heart Disease

Fetal congenital heart disease (CHD) is often associated with chromosomal abnormalities. Our primary aim was to assess stillbirth and neonatal mortality rates for pregnancies complicated by trisomies 13, 18, and 21 in the presence of CHD, from a single tertiary referral center during 2000–2020 in a...

Descripción completa

Detalles Bibliográficos
Autores principales:	Springer, Stephanie, Karner, Eva, Worda, Christof, Grabner, Maria Magdalena, Seidl-Mlczoch, Elisabeth, Laccone, Franco, Neesen, Jürgen, Scharrer, Anke, Ulm, Barbara
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410270/ https://www.ncbi.nlm.nih.gov/pubmed/36013402 http://dx.doi.org/10.3390/life12081223

Ejemplares similares

Outcome of Fetal Dysrhythmias with and without Extracardiac Anomalies
por: Springer, Stephanie, et al.
Publicado: (2023)

An efficient method for noninvasive prenatal diagnosis of fetal trisomy 13, trisomy 18, and trisomy 21
por: Sun, Xiaohan, et al.
Publicado: (2019)

Maternal prenatal screening programs that predict trisomy 21, trisomy 18, and neural tube defects in offspring
por: Chen, Yiming, et al.
Publicado: (2023)

Fetal Growth Restriction Is Associated with Pregnancy Associated Plasma Protein A and Uterine Artery Doppler in First Trimester
por: Springer, Stephanie, et al.
Publicado: (2023)

Discordant Post-natal Patterns in Fetuses With Heterotaxy Syndrome: A Retrospective Single-Centre Series on Outcome After Fetal Diagnosis
por: Seidl-Mlczoch, Elisabeth, et al.
Publicado: (2022)

Prenatal Sacrococcygeal Teratoma Diagnosed in a Fetus with Partial Trisomy 13q22
por: Dalal, Shana S., et al.
Publicado: (2019)

Performance of non-invasive prenatal testing for trisomies 21 and 18 in twin pregnancies
por: Yang, Jiexia, et al.
Publicado: (2018)

Detection of trisomies 13, 18 and 21 using non-invasive prenatal testing
por: Qiang, Rong, et al.
Publicado: (2017)

Genome-wide gene expression analysis in the placenta from fetus with trisomy 21
por: Lim, Ji Hyae, et al.
Publicado: (2017)

Expression Signature as a Biomarker for Prenatal Diagnosis of Trisomy 21
por: Volk, Marija, et al.
Publicado: (2013)

Maternal Age-Specific Rates for Trisomy 21 and Common Autosomal Trisomies in Fetuses from a Single Diagnostic Center in Thailand
por: Jaruthamsophon, Kanoot, et al.
Publicado: (2016)

Singleton exome sequencing of 90 fetuses with ultrasound anomalies revealing novel disease-causing variants and genotype–phenotype correlations
por: Smogavec, Mateja, et al.
Publicado: (2022)

Tracheal Stenosis and Congenital Heart Disease in Trisomy 21
por: Kylat, Ranjit I
Publicado: (2019)

Prenatal Isolated Ventricular Septal Defect May Not Be Associated with Trisomy 21
por: Shen, Ori, et al.
Publicado: (2014)

Noninvasive Prenatal Screening for Trisomy 21 in Patients with a Vanishing Twin
por: Kleinfinger, Pascale, et al.
Publicado: (2022)

Cost and efficacy comparison of prenatal recall and reflex DNA screening for trisomy 21, 18 and 13
por: Bestwick, Jonathan Paul, et al.
Publicado: (2019)

Altered expression of mitochondrial and extracellular matrix genes in the heart of human fetuses with chromosome 21 trisomy
por: Conti, Anna, et al.
Publicado: (2007)

Piepkorn type of osteochondrodysplasia: Defining the severe end of FLNB‐related skeletal disorders in three fetuses and a 106‐year‐old exhibit
por: Rehder, Helga, et al.
Publicado: (2018)

Beyond the Syndrome: Extensive Congenital Abnormalities in an Infant With Trisomy 21
por: Ward, Jeremy D, et al.
Publicado: (2022)

Optical Genome Mapping in Routine Human Genetic Diagnostics—Its Advantages and Limitations
por: Dremsek, Paul, et al.
Publicado: (2021)

Prenatal diagnosis of a trisomy 7/trisomy 13 mosaicism
por: Huijsdens-van Amsterdam, Karin, et al.
Publicado: (2012)

Noninvasive Prenatal Diagnosis of Fetal Trisomy 18 and Trisomy 13 by Maternal Plasma DNA Sequencing
por: Chen, Eric Z., et al.
Publicado: (2011)

Comparing Non-invasive Prenatal Testing With Invasive Testing for the Detection of Trisomy 21
por: Mokhtar, Rifat, et al.
Publicado: (2022)

Intrauterine Growth Retardation Fetus with Trisomy 16 Mosaicism
por: Chareonsirisuthigul, Takol, et al.
Publicado: (2014)

Prenatal ultrasound and magnetic resonance evaluation and fetal outcome in high‐risk fetal tumors: A retrospective single‐center cohort study over 20 years
por: Ulm, Barbara, et al.
Publicado: (2020)

Inheritance of a Chromosome 3 and 21 Translocation in the Fetuses, with One also Having Trisomy 21, in Three Pregnancies in One Family
por: Pazarbasi, A, et al.
Publicado: (2013)

Clinical evaluation of the IONA test: a non‐invasive prenatal screening test for trisomies 21, 18 and 13
por: Papageorghiou, A. T., et al.
Publicado: (2015)

Improving the calling of non-invasive prenatal testing on 13-/18-/21-trisomy by support vector machine discrimination
por: Yang, Jianfeng, et al.
Publicado: (2018)

Analysis of the impact of noninvasive prenatal testing for trisomies 21 and 18 in twin pregnancies undergoing artificial reproductive technology
por: Yang, Cuiyu, et al.
Publicado: (2022)

Fetuin A Concentration in the Second Trimester Amniotic Fluid of Fetuses with Trisomy 21 Appears to Be Lower: Phenotypic Considerations
por: Iliodromiti, S., et al.
Publicado: (2012)

Non-Invasive Prenatal Detection of Trisomy 21 Using Tandem Single Nucleotide Polymorphisms
por: Ghanta, Sujana, et al.
Publicado: (2010)

Prenatal Screening of Trisomy 21: Could Oxidative Stress Markers Play a Role?
por: Buczyńska, Angelika, et al.
Publicado: (2021)

Ultrasound, Echocardiography, MRI, and Genetic Analysis of a Fetus with Congenital Diaphragmatic Hernia and Partial 11q Trisomy
por: Fernández-Perea, Yolanda, et al.
Publicado: (2017)

Employ ductus venous blood flow in the early detection of trisomy 21, trisomy 18, and trisomy 13: A meta-analysis
por: Ge, Yibing, et al.
Publicado: (2019)

Identification and molecular characterisation of a homozygous missense mutation in the ADAMTS10 gene in a patient with Weill–Marchesani syndrome
por: Steinkellner, Hannes, et al.
Publicado: (2015)

An unusual combination of trisomy 21 and partial trisomy 5q.
por: Kim, C. J., et al.
Publicado: (1992)

New Insights into the Education of Children with Congenital Heart Disease with and without Trisomy 21
por: Schmitt, Katharina R. L., et al.
Publicado: (2023)

Recommended practice for laboratory reporting of non‐invasive prenatal testing of trisomies 13, 18 and 21: a consensus opinion
por: Deans, Zandra C., et al.
Publicado: (2017)

Non-invasive prenatal testing for the detection of trisomy 13, 18, and 21 and sex chromosome aneuploidies in 68,763 cases
por: Zhang, Yanchun, et al.
Publicado: (2022)

Combined fetal fraction to analyze the Z-score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18, and 21
por: Yang, Jiexia, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_6541cvsld0c40ksu8kqfmt5c32