Has anyone been told that you have LQT by genetic testing only and your QT interval is normal? If so, how are you treated?
Also, have you been told exactly what your genetic mutation/variation is and if the exact location of the mutation can help identify risk? I have been reading alot and it seems that some physicians are applying this new information into their bedside practice. I am wondering if your doctors talk to you about your "mutation location". If not, you should begin asking. Please share what you know about this . Thanks!




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