Using Cell-Based Therapies to Shape the Future of HLHS

Jan 19, 2016 | Suzanne Ferguson | @suzannerferguson

Here at the Todd and Karen Wanek Family Program for Hypoplastic Left Heart Syndrome, we are working on new ways to delay and even prevent heart transplants for people with congenital heart defects. In order to do that, we are studying cell-based treatments, human genetics and advanced imaging techniques along with creating the world's largest biorepository for HLHS patients and families. stem cellsmss_0000956243 In the video below, we explain in detail the exciting promise stem cells hold for the future of HLHS.

If you have any questions or are interested in our program, email us at HLHS@mayo.edu.

 


The Todd and Karen Wanek Family Program for Hypoplastic Left Heart Syndrome (HLHS) is a collaborative network of specialists bonded by the vision of delaying or preventing heart failure for individuals affected by congenital heart defects including HLHS. The specialized team is addressing the various aspects of these defects by using research and clinical strategies ranging from basic science, to diagnostic imaging to regenerative therapies.

Interested in more newsfeed posts like this? Go to the HLHS blog.

Please sign in or register to post a reply.