Abstract
Restrictive cardiomyopathy (RCM) is characterized by severely impaired ventricular relaxation with normal or near-normal systolic function and wall thickness. Etiologies of pediatric RCM are poorly understood, however sarcomeric and cytoskeletal mutations have been implicated in prior small studies. We sought to review the yield of commercially available genetic testing in children with RCM at our center.
Full Text
Published Version (
Free)
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call