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​<Return to Disease List
Meningioangiomatosis​
  • Description
  • Signalment
  • Clinical Features
  • Neurolocalization
  • Genetics
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​Meningioangiomatosis is a rare proliferative disorder of the vasculature of the CNS. It is most common in the brainstem, but unifocal and multifocal lesions have been reported in the spinal cord as well. In some animals, these lesions can be found in conjunction with other abnormal masses, such as neoplasia or hamartomas.
Age of Onset: 3 months - 14 years of age. Young animals are more commonly affected
Sex Predisposition: Any sex of animal can be affected
Clinical Course:
​Clinical signs typically worsen over time but may be highly variable based on lesion location.
Clinical Signs:
Behavioral/Mental Awareness
Seizures

Posture and Appearance
Ventral flexion of the neck
Leaning to the side
Head tilt
Anisocoria

Movement
Vestibular ataxia
Progressive tetraparesis
Spastic paresis
Circling

Proprioception
Reduced or absent conscious proprioception

Cranial Nerves
Facial nerve paralysis
Positional ventral strabismus
Positional rotary nystagmus
Diminished pupilary light reflexes

Spinal Reflexes
 
Special Reflexes (e.g. cutaneous trunci)
 
Special Functions (e.g. respiration; urination)
Fecal incontinence

​
Unknown
To read more about this disease click below:
References
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