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Muscular Dystrophy​ (Dystrophin Deficient)
  • Description
  • Signalment
  • Clinical Features
  • Neurolocalization
  • Genetics
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Muscular dystrophies are examples of degenerative myopathic conditions of both dogs and cats. These diseases are exemplified by an X-linked disease of golden retrievers and other breeds. In humans, this type of muscular dystrophy is referred to as Duchenne's muscular dystrophy.  These disease processes result from gene-associated abnormalities of a muscle membrane protein (dystrophin).
Age of Onset: 6-9 weeks of age
Sex Predisposition: Males are more commonly affected
Clinical Course:
Clinical signs may plateau after 6 months of progressive deterioration.
Clinical Signs:
Posture and Appearance
Plantigrade stance
Kyphosis to lordosis

Movement
Weakness
“Stiffness”
“Shuffling” gait
Abduction of elbows
Bunny-hopping gait
Exercise-intolerance


Cranial Nerves
Enlargement of the base of the tongue
Inability to fully open the jaw
Weak barking/dysphonia
Reduced menace response


Special Functions (e.g. respiration; urination)
Salivation
Pharyngeal and esophageal dysfunction

Muscle Atrophy
Generalized muscle atrophy (head and limb muscles)
Generalized muscle hypertrophy

Muscle Atrophy
Elevated serum muscle enzymes (CK and AST)
Diffuse neuromuscular disease
Likely to be a non-inherited spontaneous mutation
To read more about this disease click below:
References
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