CHD GENES Study
PCGC Centers are recruiting individuals of all
ages with congenital heart disease to obtain DNA as well as detailed phenotypic and
clinical data, and will follow them over time to collect outcomes data. The PCGC will
use state-of-the-art genetic techniques to interrogate the genome for single nucleotide
polymorphisms and structural variations and to conduct high-throughput, large-scale
sequencing. The biological samples, which will remain linked to detailed clinical data, will
continue to serve as a resource for long-term investigations into the genetic basis of
pediatric cardiovascular disorders. The PCGC will significantly increase understanding
of the causes and modifiers of pediatric cardiovascular pathology, and over time will
enhance early detection, treatment and prevention of congenital heart disease in newborns,
children, and adults.
Learn more about PCGC Centers
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