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Spongiform Leukoencephalomyelopathy
  • Description
  • Signalment
  • Clinical Features
  • Neurolocalization
  • Genetics
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​Spongiform leukoencephalopathy is a generalized progressive degenerative vacuolation of white matter of the brain and spinal cord.
Age of Onset: 2-9 weeks of age
Sex Predisposition: Any sex of animal can be affected
Clinical Course:
​Clinical signs worsen over time
Clinical Signs:
Behavioral/Mental Awareness
Seizures

Movement
Generalized whole-body tremors (worse in the pelvic limbs)
Ataxia
Paresis to paralysis
Limb spasticity
Rocking horse (side-to-side swaying) movement of the pelvic limbs



Proprioception
Proprioceptive deficits
​
Cranial Nerves
Absent menace response
Cranial nerve dysfunction (dropped jaw, hypoglossal dysfunction, nystagmus)
Vision and audition remain intact

Special Functions (e.g. respiration; urination)
Dysphagia
Excessive salivation

Other
Failure to grow​
DIffuse to mutlifocal CNS (White matter of the brain and spinal cord)
Autosomal recessive inheritance

For breed specific genetic testing follow the link(s) below: 
https://ofa.org/spongiform-leukoencephalomyelopathy/
https://btcoa.org/slem-dna-test/​
https://www.cagt.co.uk/product/slem/​
To read more about this disease click below:
References
Picture
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