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Related Concept Videos

Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

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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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Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy 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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Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy 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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Cardiomyopathy I: Introduction and Classification01:25

Cardiomyopathy I: Introduction and Classification

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Cardiomyopathy, or CMP, is a group of diseases affecting the myocardial structure, impairing its ability to pump blood effectively. This condition can lead to arrhythmias, heart failure, or sudden cardiac death.Cardiomyopathies are classified into primary and secondary categories:Primary Cardiomyopathy refers to conditions involving only the heart muscle that are often idiopathic (of unknown cause) or genetic. They primarily affect the myocardium without the involvement of other systemic...
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Animal Mitochondrial Genetics02:59

Animal Mitochondrial Genetics

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Among all the organelles in an animal cell, only mitochondria have their own independent genomes. Animal mitochondrial DNA is a double-stranded, closed-circular molecule with around 20,000 base pairs. Mitochondrial DNA is unique in that one of its two strands, the heavy, or H, -strand is guanine rich, whereas the complementary strand is cytosine rich and called the light, or L, -strand. Compared to nuclear DNA, mitochondrial DNA has a very low percentage of non-coding regions and is marked by...
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A Doxorubicin-Induced Murine Model of Dilated Cardiomyopathy In Vivo
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Dilated cardiomyopathy in a De Brazza's monkey (Cercopithecus neglectus).

Alena Felkai1, Larry Vogelnest, Suzanne McNabb

  • 1Petersham, New South Wales, Australia.

Journal of Medical Primatology
|March 12, 2014
PubMed
Summary

Dilated cardiomyopathy caused heart failure in a De Brazza's monkey. This led to lung complications, highlighting the severe impact of cardiac disease in primates.

Keywords:
decreased myocardial contractionheart failureinappetencenon-human primatepleural effusionweight loss

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Area of Science:

  • Veterinary Cardiology
  • Primate Medicine
  • Comparative Pathology

Background:

  • Cardiomyopathies are observed in various primate species.
  • Potential causes include infection, nutritional issues, genetics, toxins, or idiopathic factors.
  • Idiopathic cardiomyopathies are common in primates.

Observation:

  • A De Brazza's monkey (Cercopithecus neglectus) exhibited symptoms of weight loss and inappetence.
  • Diagnostic procedures included physical examination, blood work, imaging, and electrocardiography.
  • The animal presented with clinical signs suggestive of systemic illness.

Findings:

  • Radiographs and echocardiogram showed pleural effusion, lung collapse, cardiomegaly, and reduced myocardial contractility.
  • Necropsy confirmed pulmonary infarction secondary to heart failure.
  • The primary diagnosis was dilated cardiomyopathy.

Implications:

  • This case underscores the importance of recognizing cardiac disease in non-human primates.
  • Dilated cardiomyopathy can lead to severe complications such as pulmonary infarction.
  • Further research into primate cardiomyopathies is warranted for improved diagnostics and treatment.