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ARVD/C is an inherited disorder and one of the most common causes of sudden death in athletes and young, apparently healthy adults. Its prevalence is estimated at one in 5,000 people. The disorder ...
In 1996, ARVD/C was added to the WHO classification of cardiomyopathies. The name is derived from the observation that electrical disturbances of the heart (arrhythmogenic) are common and tend to ...
ARVD/C is an inherited disorder and one of the most common causes of sudden death in athletes and young, apparently healthy adults. Its prevalence is estimated at one in 5,000 people.
The high rate of recurrence, say investigators, calls into question the early use of catheter ablation as an effective antiarrhythmic strategy in patients with arrhythmogenic right ventricular ...
Most people with ARVD/C don’t know they have it until they experience symptoms as young adults, including a heart rhythm abnormality, heart failure, or even sudden cardiac arrest due to arrhythmias ...
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is challenging to diagnose because of nonspecific findings, particularly in the early phases of the disease. Clinical diagnosis ...
Conclusions We describe a patient with cardiac sarcoidosis who was diagnosed with ARVD/C on the basis of his clinical symptoms and electrocardiography findings. Diagnosis of cardiac sarcoidosis ...
In this study, researchers used an ARVD/C patient's skin cells to make induced pluripotent stem cells. Then they used those stem cells to generate ARVD/C patient-specific heart cells (shown here ...
ARVD/C affects fewer than 1 in 1,000 Americans but is responsible for a fifth of all sudden cardiac deaths among people under 35 years old. For Rock-Torcivia, its effects have been drastic: After ...
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