scholarly journals P25.02: Beneficial effect of prenatal diagnosis of congenital heart defects over a ten year period in a referral center

2009 ◽  
Vol 34 (S1) ◽  
pp. 272-272
Author(s):  
P. M. van Brussel ◽  
J. Ottenkamp ◽  
C. Bilardo ◽  
S. B. Clur
Keyword(s):  
Prenatal Diagnosis ◽  
Beneficial Effect ◽  
Congenital Heart Defects ◽  
Congenital Heart ◽  
Heart Defects ◽  
Referral Center

Four-year experience with prenatal diagnosis of congenital heart defects at a single referral center in Japan with focus on inaccurately diagnosed cases

2012 ◽  
Vol 39 (4) ◽  
pp. 235-240 ◽  
Author(s):  
Yukako Yoshikane ◽  
Toshiyuki Yoshizato ◽  
Yoshiko Otake ◽  
Naoki Fusazaki ◽  
Hirotsugu Obama ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Congenital Heart Defects ◽  
Congenital Heart ◽  
Heart Defects ◽  
Referral Center

Immediate and long-term outcomes in children with prenatal diagnosis of selected isolated congenital heart defects

2007 ◽  
Vol 29 (1) ◽  
pp. 38-43 ◽  
Author(s):  
I. B. Fuchs ◽  
H. Müller ◽  
H. Abdul-Khaliq ◽  
T. Harder ◽  
J. W. Dudenhausen ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Congenital Heart Defects ◽  
Congenital Heart ◽  
Heart Defects ◽  
Long Term Outcomes

Prenatal Diagnosis of Congenital Heart Defects in Thoracoabdominally Conjoined Twins

1985 ◽  
Vol 313 (6) ◽  
pp. 370-374 ◽  
Author(s):  
Stephen P. Sanders ◽  
Alvin J. Chin ◽  
Ira A. Parness ◽  
Beryl Benacerraf ◽  
Michael F. Greene ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Congenital Heart Defects ◽  
Congenital Heart ◽  
Heart Defects ◽  
Conjoined Twins

scholarly journals PRENATAL DIAGNOSIS OF CONGENITAL HEART DEFECTS: DOES IT MAKE A DIFFERENCE IN SURVIVAL?

2013 ◽  
Vol 61 (10) ◽  
pp. E476
Author(s):  
Matthew Oster ◽  
Christopher H. Kim ◽  
Aaron S. Kusano ◽  
Janet D. Cragan ◽  
Paul B. Dressler ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Congenital Heart Defects ◽  
Congenital Heart ◽  
Heart Defects

scholarly journals Prenatal diagnosis of congenital heart defects: accuracy and discrepancies in a multicenter cohort

2016 ◽  
Vol 47 (5) ◽  
pp. 616-622 ◽  
Author(s):  
C. L. van Velzen ◽  
S. A. Clur ◽  
M. E. B. Rijlaarsdam ◽  
E. Pajkrt ◽  
C. J. Bax ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Congenital Heart Defects ◽  
Congenital Heart ◽  
Heart Defects ◽  
Multicenter Cohort

Potential role of “omics” technique in prenatal diagnosis of congenital heart defects

2018 ◽  
Vol 482 ◽  
pp. 185-190
Author(s):  
Lizhu Chen ◽  
Johnny Guan ◽  
Qiuju Wei ◽  
Zhengwei Yuan ◽  
Mo Zhang
Keyword(s):  
Prenatal Diagnosis ◽  
Congenital Heart Defects ◽  
Congenital Heart ◽  
Potential Role ◽  
Heart Defects

scholarly journals Utility of Fetal Cardiovascular Magnetic Resonance for Prenatal Diagnosis of Complex Congenital Heart Defects

2021 ◽  
Vol 4 (3) ◽  
pp. e213538 ◽  
Author(s):  
Daniel Salehi ◽  
Katrin Fricke ◽  
Misha Bhat ◽  
Håkan Arheden ◽  
Petru Liuba ◽  
...  
Keyword(s):  
Cardiovascular Magnetic Resonance ◽  
Prenatal Diagnosis ◽  
Magnetic Resonance ◽  
Congenital Heart Defects ◽  
Congenital Heart ◽  
Heart Defects

scholarly journals Prenatal Diagnosis by Array Comparative Genomic Hybridization in Fetuses with Cardiac Abnormalities

Genes ◽  
2021 ◽  
Vol 12 (12) ◽  
pp. 2021
Author(s):  
Katarzyna Kowalczyk ◽  
Magdalena Bartnik-Głaska ◽  
Marta Smyk ◽  
Izabela Plaskota ◽  
Joanna Bernaciak ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Comparative Genomic Hybridization ◽  
Congenital Heart Defects ◽  
Congenital Heart ◽  
Array Cgh ◽  
Heart Diseases ◽  
Heart Defects ◽  
Comparative Genomic ◽  
Genomic Hybridization ◽  
Fetal Ultrasound

Congenital heart defects (CHDs) appear in 8–10 out of 1000 live born newborns and are one of the most common causes of deaths. In fetuses, the congenital heart defects are found even 3–5 times more often. Currently, microarray comparative genomic hybridization (array CGH) is recommended by worldwide scientific organizations as a first-line test in the prenatal diagnosis of fetuses with sonographic abnormalities, especially cardiac defects. We present the results of the application of array CGH in 484 cases with prenatally diagnosed congenital heart diseases by fetal ultrasound scanning (256 isolated CHD and 228 CHD coexisting with other malformations). We identified pathogenic aberrations and likely pathogenic genetic loci for CHD in 165 fetuses and 9 copy number variants (CNVs) of unknown clinical significance. Prenatal array-CGH is a useful method allowing the identification of all unbalanced aberrations (number and structure) with a much higher resolution than the currently applied traditional assessment techniques karyotype. Due to this ability, we identified the etiology of heart defects in 37% of cases.

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