| Literature DB >> 33295458 |
Silméia Garcia Zanati Bazan1, Gilberto Ornellas de Oliveira1, Caroline Ferreira da Silva Mazeto Pupo da Silveira1, Fabrício Moreira Reis1, Karina Nogueira Dias Secco Malagutte1, Lucas Santos Nielsen Tinasi1, Rodrigo Bazan1, João Carlos Hueb1, Katashi Okoshi1.
Abstract
Hypertrophic cardiomyopathy (HCM) is the most common heart disease with a genetic origin, and its main characteristic is left ventricular hypertrophy that occurs in the absence of other conditions that trigger this change. HCM may present from asymptomatic forms to manifestations of sudden cardiac death and severe heart failure. Contemporary high-resolution imaging methods and more accurate clinical scores have been used and developed to provide a prognostic assessment and adequate functional assessments, as well as to allow for the stratification of clinical severity. These aspects will be addressed in this review, along with other classic topics inherent to the study of this disease.Entities:
Mesh:
Year: 2020 PMID: 33295458 DOI: 10.36660/abc.20190802
Source DB: PubMed Journal: Arq Bras Cardiol ISSN: 0066-782X Impact factor: 2.000