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Sphingomyelinosis (Niemann Pick Type C)   ​
  • Description
  • Signalment
  • Clinical Features
  • Neurolocalization
  • Genetics
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Sphingomyelinosis is a lipid storage disorder characterized by a lack of sphingomyelinase resulting in excess sphingomyelin accumulation within the central nervous and reticuloendothelial systems.
Age of Onset: 2-4 months of age
Sex Predisposition: Any sex of animal can be affected
Clinical Course:
Clinical signs progress over the course of several months
Clinical Signs:
Behavioral/Mental Awareness
Stupor
​Paropsis
​

Movement
Ataxia
Hypermetria
Head tremor

Proprioception
Proprioceptive deficit

Cranial Nerves
Nystagmus
Loss of equilibrium/balance
Diffuse intracranial
Unknown
To read more about this disease click below:
References
Picture
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