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Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...
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05:14A Doxorubicin-Induced Murine Model of Dilated Cardiomyopathy In Vivo
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Described is a protocol to establish a Doxorubicin-induced dilated cardiomyopathy (DCM) model in mice via long-term intraperitoneal injection of...
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01:30Socioemotional Development during Infancy
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Socio-emotional development in infancy is primarily shaped by early emotional responses and social connections, with temperament playing a central role. Temperament refers to the consistent patterns in an individual's emotional and behavioral responses, observable even in infancy. By examining temperament, researchers can better understand an infant's unique ways of interacting with the world, influencing subsequent personality and socio-emotional growth.
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01:29Cardiomyopathy IV: Restrictive Cardiomyopathy
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Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...
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01:29Cardiomyopathy III: Hypertrophic Cardiomyopathy
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Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
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10:08Tachycardia-Induced Cardiomyopathy As a Chronic Heart Failure Model in Swine
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01:30
Cardiomyopathy II: Dilated Cardiomyopathy
Published on: June 19, 2025
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[Two cases with dilated cardiomyopathy since infancy]
1Department of Vasculocardiology, Children's Hospital Affiliated to Zhengzhou University/Children's Hospital of Henan Province, Zhengzhou 450018, China.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|September 19, 2019
Summary
No abstract available in PubMed .