Dilated cardiomyopathy: clinical and molecular genetic preconditions
Keywords:
кардиомиопатии
генетические причины
ламин
саркомерные белки
клинические особенности
дистрофин
десмин
структурные белки
cardiomyopathies
genetic causes
lamin
sarcomeric proteins
clinical features
dystrophin
desmin
structural proteins
Abstract
The article examines the genetic causes of the development of some hereditary forms of cardiomyopathies associated with gene mutations, as well as the relationship of genetic mutations with clinical manifestations. Complications, main methods of diagnosis and treatment of dilated cardiomyopathy, aspects of differential diagnosis with other myocardial diseases are considered.
