Maternal plasma mRNA species in fetal heart defects: a potential for molecular screening

2016 ◽  
Vol 36 (8) ◽  
pp. 738-743 ◽  
Author(s):  
Alessandra Curti ◽  
Cristina Lapucci ◽  
Silvia Berto ◽  
Daniela Prandstraller ◽  
Antonella Perolo ◽  
...  
2010 ◽  
Vol 29 (11) ◽  
pp. 1573-1580 ◽  
Author(s):  
Jimmy Espinoza ◽  
Wesley Lee ◽  
Christine Comstock ◽  
Roberto Romero ◽  
Lami Yeo ◽  
...  

2020 ◽  
Vol 69 (2) ◽  
pp. 43-50
Author(s):  
Viktoria A. Lim

Hypothesis/aims of study. Fetal heart defects are the most common malformations causing infant mortality. The task of the obstetric care service is to make a timely diagnosis, which includes high-quality ultrasound screening and, if necessary, fetal echocardiography. This study aimed to compare fetal echocardiography with postpartum echocardiography. Study design, materials and methods. 101 pregnant women with both isolated fetal heart defects and combined pathology were examined for the period 20172019. Results. The greatest number of heart defects was detected at 2331 weeks of gestation. The structure of the malformations is diverse, the most common one being a complete form of the atrioventricular canal defect. In multiple pregnancies, complex heart defects were often combined with abnormalities in other organ systems. Conclusion. It is recommended to describe the heart structure in detail from 2122 weeks of pregnancy. If cardiac pathology is detected in utero, it is mandatory to conduct an examination of other fetal organs.


2019 ◽  
Vol 47 (3) ◽  
pp. 188-197
Author(s):  
Nelangi M. Pinto ◽  
Kevin A. Henry ◽  
Guo Wei ◽  
Xiaoming Sheng ◽  
Tom Green ◽  
...  

2011 ◽  
Vol 204 (1) ◽  
pp. S259-S260
Author(s):  
Priyadarshini Koduri ◽  
Maria Adelaida Giraldo ◽  
Phillip Shlossman ◽  
Anthony Sciscione ◽  
Vincenzo Berghella ◽  
...  

Author(s):  
Dena Towner

ABSTRACT Congenital cardiac abnormalities are one of the most common birth defects at 1 in 120 births. The majority of which have no underlying risk factors. The fetal heart assessment is felt to be the most challenging part of the anatomy examination and most studies report that nearly half of major heart defects are missed, thus, confirming the challenge for antenatal detection rate. This article reviews the key views and key items to assess in fetal heart imaging during the anatomy ultrasound. How to cite this article Towner D. Optimizing Fetal Heart Screening at the Anatomy Ultrasound. Donald School J Ultrasound Obstet Gynecol 2016;10(1):50-54.


2019 ◽  
Vol 220 (1) ◽  
pp. 104.e1-104.e15 ◽  
Author(s):  
Takekazu Miyoshi ◽  
Hiroshi Hosoda ◽  
Michikazu Nakai ◽  
Kunihiro Nishimura ◽  
Mikiya Miyazato ◽  
...  

2004 ◽  
Vol 15 (4) ◽  
pp. 327-341 ◽  
Author(s):  
LINDSEY ALLAN

Ultrasound has been used in cardiac diagnosis since the 1960s. The original modality used was M-mode, which recorded the movement of heart structures relative to a single line of sound passed through the heart and was displayed as a paper tracing. During the 1970s, a two-dimensional image became possible, but it was a static image, which had limited value for cardiac evaluation. However, by the end of the 1970s, advances in ultrasound equipment allowed the heart to be displayed in real-time. This technology was applied initially in the adult and subsequently in the child. Echocardiography proved particularly suitable for children, partly because it is non-invasive and repeatable, but also because most heart disease in children is due to malformation of anatomical structure, which ultrasound can ideally display. At the same time, obstetric ultrasound was progressing rapidly and descriptions of the appearances of malformations in most fetal systems began to be published by the end of the 1970s. It was not until real-time equipment became generally available in obstetrics that the fetal heart could be satisfactorily evaluated. This led to descriptions by several authors of normal fetal cardiac anatomy as seen echocardiographically in 1980. The appearances of the echocardiogram in different forms of congenital heart disease (CHD) in children were published in the late 1970's, setting the stage for diagnosis in fetal life. As a result, by the mid-1980's, most major forms of CHD had been detected prenatally.


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