Syndromic and Metabolic Cardiomyopathies

Mit változtat a diagnózis

Knowing about it supports rhythm monitoring, as some people need a pacemaker or treatment of an accessory pathway.

Vizsgált gének

Más néven

PRKAG2 cardiac syndrome; PRKAG2 cardiomyopathy; PRKAG2 syndrome

Mit változtat a diagnózis

Knowing about it supports regular rhythm monitoring, as conduction disease can progress and need a pacemaker.

Vizsgált gének

Más néven

NKX2-5-related congenital, conduction and myopathic heart disease

Vizsgált gének

Más néven

ACTN2 familial isolated dilated cardiomyopathy; cardiomyopathy, dilated, 1AA, with or without LVNC; cardiomyopathy, hypertrophic, 23, with or without LVNC; CMD1AA; dilated cardiomyopathy 1AA with or without left ventricular noncompaction; dilated cardiomyopathy type 1AA; familial isolated dilated cardiomyopathy caused by mutation in ACTN2

Vizsgált gének

Vizsgált gének

Más néven

cardiomyopathic mitochondrial DNA depletion syndrome 10; cataract and cardiomyopathy; mitochondrial DNA depletion syndrome 10

Vizsgált gének

Más néven

mitochondrial DNA depletion syndrome 12; mitochondrial DNA depletion syndrome 12 (cardiomyopathic type); mitochondrial DNA depletion syndrome 12B (cardiomyopathic type) AR; mitochondrial DNA depletion syndrome type 12; MTDPS12; MTDPS12B

Vizsgált gének

Más néven

mitochondrial DNA depletion syndrome 12A (cardiomyopathic type) AD; mitochondrial DNA depletion syndrome 12a (cardiomyopathic type), autosomal dominant; mitochondrial DNA depletion syndrome 12a (cardiomyopathic type), autosomal dominant; MTDPS12A; MTDPS12A