We actively support scientific studies and creation of a database for research focused on Situs Inversus and related rare conditions aiming to uncover the genetic components and connections not previously explored.
Presently, there are only 7 open studies world wide for Situs Inversus, Dextrocardia, Heterotaxy, Primary Ciliary Dyskinesia (PCD), and Kartagener Syndrome. This study is actively recruiting for molecular genetic of heterotaxy and related congenital heart defects.
We collaborate with the head researcher and here are some details on this study: it is FREE. People can enroll who are both domestic and international. They will intake your medical and family history. Medical records will be sent to them. They will mail you the materials for the study such as genetic lab work tubes or cheek swabs for DNA analysis. The blood work will be drawn at a lab near you, and the cost will be only for the venipuncture/lab draw to be performed which they reimburse participants with gift card vouchers. This study is inclusive of children, adults, or relatives. This study is NIH/grant funded and their team is incredibly responsive. See if you can help contribute to the future of genetic testing and counseling as well as knowledge about the biology of normal and abnormal development of left-right asymmetry!
Molecular Genetics of Heterotaxy and Related Congenital Heart Defects
