Congenital heart diseases are a common prenatal finding. The prenatal identification of an
associated genetic syndrome or a major extracardiac anomaly helps to understand the …

Congenital Heart Disease: Prenatal Diagnosis and Genetic Ass... : Obstetrical & Gynecological
Survey Congenital Heart Disease: Prenatal Diagnosis and Genetic Associations : Obstetrical …

Congenital heart disease affects around 0.7% of liveborn infants and is the most frequent
cause of death from congenital malformations. This review will consider some of the …

The information in this review provides insights into the state-of-the-art knowledge about the
molecular genetic causes of congenital heart defects. It suggests that DNA testing may …

Recent research has demonstrated that genetic alterations or variations contribute
considerably to the development of congenital heart disease. Many kinds of genetic tests are …

The recent exponential increase in the knowledge of genetics has revolutionized the
understanding of congenital heart diseases (CHDs) during the past few decades. Prior …

Objective Determine prenatal detection rate, mortality and association with genetic
abnormalities in patients with severe CHD. Method Single center retrospective study in …

Cardiomyopathies are diseases of the heart muscle with variable clinical expressivity. Most
of forms are inherited as dominant trait, and with incomplete penetrance until adulthood …

Prenatal identification and management of fetal cardiac abnormalities are important
because congenital anomalies are a leading cause of infant death, and congenital heart …

Background Most congenital heart defects (CHDs) are diagnosed on targeted prenatal
transvaginal (TVS) or transabdominal (TAS) ultrasonography during the early second …