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Lipid Storage Myopathy
  • Description
  • Signalment
  • Clinical Features
  • Neurolocalization
  • Genetics
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Lipid storage myopathy is an idiopathic metabolic disorder characterized by abnormal accumulation of lipids within muscle fibers.
Age of Onset: Less than 6 years of age
Sex Predisposition: Any sex of animal can be affected
Clinical Course:
​Clinical signs worsen over the course of several weeks to months
Clinical Signs:
Behavioral/Mental Awareness
Depressed

Movement
Difficulty walking
Weakness

Painful Reactions
Pain on palpation of the cervical, thoracic, and lumbar spine
Pain on palpation of appendicular muscles

Diffuse myalgia

Muscle Atrophy
Pelvic limb muscle atrophy

Diffuse muscle
Unknown
To read more about this disease click below:
References
Picture
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