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Recommends genetic testing and multidisciplinary care in prenatal congenital heart disease, indicating optimized maternal and neonatal outcomes.
When CHD is identified through prenatal screening, patients should be referred for genetic counseling and offered appropriate genetic testing. Prenatal diagnosis of genetic syndromes related to CHD and close communication between obstetric, genetic, and pediatric providers can help optimize outcomes for both mother and baby.
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Hopkins et al. (2019) studied this question.
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