Population
Patients with autosomal recessive atrial dilated cardiomyopathy associated with homozygous mutation of the…
Design
Other
Authors
Loading...
Supports consideration of NPPA-related atrial cardiomyopathy in unexplained dilatation with thromboembolism; hypothesis-generating for targeted interventions.
Autosomal recessive atrial dilated cardiomyopathy is a rare genetic disorder linked to NPPA mutations, presenting with extreme atrial dilatation, atrial standstill, and thromboembolic risk despite preserved LV function.
Disertori et al. (2012) studied this question.
Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context: