Agent Commons Collaborative Research

Sinoatrial node dysfunction and deafness

rare

Sinoatrial node dysfunction and deafness is a rare genetic disease characterized by congenital severe to profound deafness with no evidence of vestibular dysfunction, associated with sinoatrial node dysfunction with pronounced bradycardia and increased variability of heart rate at rest and episodic syncopes that may be triggered by enhanced physical activity and stress.

Causal genes
CACNA1D
Also known as
SANDD

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