Hypertrophic cardiomyopathy: A review

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dc.contributor.authorBazan, Silméia Garcia Zanati [UNESP]
dc.contributor.authorde Oliveira, Gilberto Ornellas [UNESP]
dc.contributor.authorda Silveira, Caroline Ferreira da Silva Mazeto Pupo [UNESP]
dc.contributor.authorReis, Fabrício Moreira [UNESP]
dc.contributor.authorMalagutte, Karina Nogueira Dias Secco [UNESP]
dc.contributor.authorTinasi, Lucas Santos Nielsen [UNESP]
dc.contributor.authorBazan, Rodrigo [UNESP]
dc.contributor.authorHueb, João Carlos [UNESP]
dc.contributor.authorOkoshi, Katashi [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2021-06-25T11:08:38Z
dc.date.available2021-06-25T11:08:38Z
dc.date.issued2020-11-01
dc.description.abstractHypertrophic 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.en
dc.description.affiliationUniversidade Estadual Paulista Júlio de Mesquita Filho Faculdade de Medicina de Botucatu UNESP
dc.description.affiliationUnespUniversidade Estadual Paulista Júlio de Mesquita Filho Faculdade de Medicina de Botucatu UNESP
dc.format.extent927-935
dc.identifierhttp://dx.doi.org/10.36660/abc.20190802
dc.identifier.citationArquivos Brasileiros de Cardiologia, v. 115, n. 5, p. 927-935, 2020.
dc.identifier.doi10.36660/abc.20190802
dc.identifier.fileS0066-782X2020001300927.pdf
dc.identifier.issn1678-4170
dc.identifier.issn0066-782X
dc.identifier.scieloS0066-782X2020001300927
dc.identifier.scopus2-s2.0-85097500104
dc.identifier.urihttp://hdl.handle.net/11449/208231
dc.language.isoeng
dc.language.isopor
dc.relation.ispartofArquivos Brasileiros de Cardiologia
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectCardiomyopathy, hypertrophic/genetics
dc.subjectEchocardiography/methods
dc.subjectHeart failure
dc.subjectHypertrophy, left ventricle
dc.subjectSudden cardiac death
dc.titleHypertrophic cardiomyopathy: A reviewen
dc.titleCardiomiopatia Hipertrófica – Revisãopt
dc.typeResenha

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Artigos - Neurologia, Psicologia e Psiquiatria - FMB
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