Calmodulinopathy is a novel, life-threatening clinical entity affecting young individuals that requires further research to decipher disease mechanisms and identify novel therapies.
Calmodulinopathy is a newly recognized, severe genetic arrhythmia syndrome affecting the young, characterized by mutations in CALM genes and a high risk of sudden cardiac death that often fails to respond to conventional antiarrhythmic treatments.
Absolute Event Rate: 0% vs 0%
, decipher disease mechanisms and identify novel therapies.
Kotta et al. (Thu,) reported a other. Calmodulinopathy is a novel, life-threatening clinical entity affecting young individuals that requires further research to decipher disease mechanisms and identify novel therapies.