Dilated cardiomyopathy (Q42359): Difference between revisions
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Cardiomiopatia dilatada é um transtorno do miocárdio no qual há disfunção sistólica e dilatação da câmara de um ou ambos os ventrículos na ausência de uma causa hemodinâmica que possa produzir a dilatação e disfunção existentes, incluindo causas fisiológicas (como sepse) ou anatômicas seja com condições anormais de carga (como coarctação da aorta) ou isquemia (como doença arterial coronariana ou anomalias). _x000D_ _x000D_ Informações adicionais: Condições fisiológicas e anatômicas podem afetar o fenótipo morfofuncional da cardiomiopatia dilatada. Se este fenótipo morfofuncional for mantido após intervenção apropriada, então uma cardiomiopatia dilatada está estabelecida. | |||
| description / en | description / en | ||
Dilated cardiomyopathy is a myocardial disorder in which there is systolic dysfunction and chamber dilation of one or both ventricles in the absence of a haemodynamic cause that can produce the existent dilation and dysfunction, including physiological (such as sepsis) or anatomic causes with either abnormal loading conditions (such as coarctation of the aorta) or ischaemia (such as coronary artery disease or anomalies). Additional information: Physiological and anatomic conditions can affect the dilated cardiomyopathy morphofunctional phenotype. If this morphofunctional phenotype is retained after appropriate intervention, then a dilated cardiomyopathy is established. | |||
Revision as of 08:50, 13 August 2026
Dilated cardiomyopathy is a myocardial disorder in which there is systolic dysfunction and chamber dilation of one or both ventricles in the absence of a haemodynamic cause that can produce the existent dilation and dysfunction, including physiological (such as sepsis) or anatomic causes with either abnormal loading conditions (such as coarctation of the aorta) or ischaemia (such as coronary artery disease or anomalies). Additional information: Physiological and anatomic conditions can affect the dilated cardiomyopathy morphofunctional phenotype. If this morphofunctional phenotype is retained after appropriate intervention, then a dilated cardiomyopathy is established.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | BC43.0 |
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| English | Dilated cardiomyopathy |
Dilated cardiomyopathy is a myocardial disorder in which there is systolic dysfunction and chamber dilation of one or both ventricles in the absence of a haemodynamic cause that can produce the existent dilation and dysfunction, including physiological (such as sepsis) or anatomic causes with either abnormal loading conditions (such as coarctation of the aorta) or ischaemia (such as coronary artery disease or anomalies). Additional information: Physiological and anatomic conditions can affect the dilated cardiomyopathy morphofunctional phenotype. If this morphofunctional phenotype is retained after appropriate intervention, then a dilated cardiomyopathy is established. |
