LMNA-related dilated cardiomyopathy


A case of idiopathic dilated cardiomyopathy (DCM) that is likely to be associated with LMNA mutation Arg190Pro in a heterozygote is described. The features of DCM in the patient were conduction disorders, cardiac arrhythmias, progressive heart failure and minor musculoskeletal disturbances. We consider that the mutation Arg190Pro contributes to the… (More)
DOI: 10.1093/omcr/omu040

1 Figure or Table


  • Presentations referencing similar topics