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Cytogenomics of Cardiovascular Malformations Consortium Registry

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Updated on 19 February 2024

Summary

The purpose of this study is to identify submicroscopic chromosomal imbalances, termed copy number variations (CNV), which are associated with the development of congenital heart defects (CHD) and cardiovascular malformations and to establish a large de-identified database of chromosome microarray abnormalities in patients with CHD.

Description

The purpose of this study is to identify submicroscopic chromosomal imbalances, termed copy number variations (CNV), which are associated with the development of congenital heart defects (CHD) and cardiovascular malformations and to establish a large de-identified database of chromosome microarray abnormalities in patients with CHD.

Details
Condition Cardiovascular Malformation
Age 100years or below
Clinical Study IdentifierTX4222
Last Modified on19 February 2024

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