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Muscular Dystrophy (Atrioventricular)
  • Description
  • Signalment
  • Clinical Features
  • Neurolocalization
  • Genetics
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Atrioventricular muscular dystrophy is an inherited disease resulting in fibrous replacement of cardiomyocytes beginning in the atria and progressively involving the ventricles.
Age of Onset: 1-3 years of age
Sex Predisposition: Males are more commonly affected
Clinical Course:
​Clinical signs typically progress to result in congestive heart failure within months.
Clinical Signs:
Behavioral/Mental Awareness
Syncopal episodes
​

Special Functions (e.g. respiration; urination)
Bradycardia
3rd degree AV block (non-responsive to atropine)

Muscle Atrophy
Muscular dystrophy of facial and shoulder muscles​
Diffuse neuromuscular
Unknown
To read more about this disease click below:
References
Picture
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