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Necrotizing Leukoencephalomyelitis (NLE)
  • Description
  • Signalment
  • Clinical Features
  • Neurolocalization
  • Genetics
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Necrotizing leukoencephalomyelitis (NLE) is a non-infectious inflammatory condition under the spectrum of meningoencephalitis of unknown origin. In NLE, the lymphoplasmacytic inflammation is primarily distributed throughout the deep cerebral white matter and diencephalon. The inflammation can be distributed bilaterally, but is often worse in one hemisphere.
Age of Onset: 1-5 years of age most commonly (some reports cite disease onset >5 years of age)
Sex Predisposition: Any sex of animal can be affected
Clinical Course:
​Clinical signs often present acutely and progress over the course of several months
Clinical Signs:
Behavioral/Mental Awareness 
**Generalized seizures 
Behavioral changes 
Compulsive pacing
Head pressing
​Depression

 
Posture and Appearance
Opisthotonous

Movement 
Head turning and circling
**Ataxia/Abnormal gait
Tetraparesis


Proprioception 
Proprioceptive deficit (contralateral) 
 
Cranial Nerves 
Facial hypalgesia (contralateral) 
Menace deficit (contralateral) 
Central vestibular signs (**head tilt, nystagmus, vestibular strabismus)
Anisocoria
​Reduced olfaction
​
Intracranial - Prosencephalon (deep white matter and diencephalon)
Unknown
To read more about this disease click below:
References
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