Dilated cardiomyopathy: clinical and molecular genetic preconditions

  • Кристина Сергеевна Ворганова Saint-Petersburg State Pediatric Medical University 194100, Saint-Рetersburg
Keywords: 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.

Author Biography

Кристина Сергеевна Ворганова, Saint-Petersburg State Pediatric Medical University 194100, Saint-Рetersburg
Litovskaya str., 2; Clinical Resident of the Department of Faculty Therapy named after Professor V.A. Waldman
Published
2021-10-22
How to Cite
Ворганова, К. С. (2021). Dilated cardiomyopathy: clinical and molecular genetic preconditions. University Therapeutic Journal, 3(2), 64-72. Retrieved from https://ojs3.gpmu.org/index.php/Un-ther-journal/article/view/2960
Section
Статьи