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CLARITY
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Research participants wanted for The Collaborative For Longitudinal Aortic Imaging In The Young (CLARITY):


Are you interested in helping researchers develop the world’s largest database for children and young adults with genetic aortic disease? Researchers at Texas Children’s Hospital are interested in learning more about young people with aortic disease that has a genetic basis. They are asking for your help because there are currently no medical guidelines on how to best manage aortic dilation in children, and little is known about the long-term outcomes of these genetic conditions. In an effort to learn more, researchers will collect clinical information from your medical records to better understand how the aorta changes over time, and how your genotype (your unique genetic code) affects your disease. This information will help create guidelines that will provide better tools for doctors to diagnose, estimate risks, and treat children and young adults with genetic aortic disease. These guidelines aim to improve the care and quality of life for individuals diagnosed with these conditions.

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Medical disclaimer:  The information provided on this resource page is for educational purposes only and should not be considered medical advice. It is intended to offer general information about neonatal Marfan syndrome and related topics for parents, families, and healthcare professionals. This information is not a substitute for professional medical evaluation, diagnosis, or treatment. Read full medical disclaimer here.

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