Literature DB >> 33295458

Hypertrophic Cardiomyopathy: A Review.

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.

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Year:  2020        PMID: 33295458     DOI: 10.36660/abc.20190802

Source DB:  PubMed          Journal:  Arq Bras Cardiol        ISSN: 0066-782X            Impact factor:   2.000


  1 in total

1.  Echocardiography Guiding Percutaneous Treatment of Obstructive Hypertrophic Cardiomyopathy: Navigating (In Known Waters) Is Necessary.

Authors:  Minna Moreira Dias Romano
Journal:  Arq Bras Cardiol       Date:  2022-05       Impact factor: 2.667

  1 in total

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