Meet the team! – Leo Dean Jansen, MD
Together we can find a cure for PLN genetic heart disease
Leo Dean Jansen, MD, Board Member North American PLN Foundation:
“Prior to my PLN diagnosis, I had a busy surgical orthopedic practice, traveled extensively with my family and participated in many sports activities. Now it is very difficult not being able to do all those things I loved. Fortunately, working with the PLN foundation has allowed me to regain some purpose in my life. I have nine family members with the PLN mutation which makes me even more committed to finding a cure. As a Board Member, I am involved in education and fundraising for the foundation. I have also given talks at scientific meetings on PLN heart disease from a patient/physician perspective”.