We use our own and third party cookies to offer you our services, customize and analyze your browsing and show you advertising related to your preferences. By continuing to browse, we consider that you accept its use. You can change the settings and get more information in the
Today, thanks to advances in molecular diagnostics, it is currently possible to identify the underlying genetic cause of many of these diseases. This genetic diagnosis makes it possible to confirm diagnostic suspicions, to assess the risk of adverse events in some cases, and to rule out whether a family member is a carrier of the genetic predisposition.
A comprehensive assessment is essential in all cases. This includes genetic information with a clinical assessment to show the degree of individual affectation. For this, and depending on the pathology, we use diagnostic tests that include imaging techniques (echocardiogram, resonance, tomography), stress tests, prolonged cardiac rhythm monitoring, electrophysiological studies, heart biopsy, etc.
We are sorry, we are working to improve PortalCLÍNIC. Help us become better, tell us why
Thanks for your help!
An error has occurred and we were unable to send your opinion, please try again later.
The donations that can be done through this webpage are exclusively for the benefit of Hospital Clínic of Barcelona through Fundació Clínic per a la Recerca Biomèdica and not for BBVA Foundation, entity that collaborates with the project of PortalClínic.
Receive the latest updates related to this content.
Thank you for subscribing!
If this is the first time you subscribe you will receive a confirmation email, check your inbox
An error occurred and we were unable to send your data, please try again later.