Familial Restrictive Cardiomyopathy 1 (TNNI3)
Autoszomális domináns
A form of restrictive cardiomyopathy caused by changes in the sarcomere gene TNNI3.
Mit változtat a diagnózis
Knowing about it supports specialist heart monitoring and screening of relatives.
Vizsgált gének
Más néven
cardiomyopathy, familial restrictive, type 1; familial isolated restrictive cardiomyopathy caused by mutation in TNNI3; RCM1; TNNI3 familial isolated restrictive cardiomyopathy
