VNDD
  • Home
  • Search
  • Methodology
  • Contact
<Return to Disease List
Fibrinoid Leukodystrophy (Fibrinoid Encephalomyelopathy/Alexander Disease/Rosenthal Fiber Myelopathy)​
  • Description
  • Signalment
  • Clinical Features
  • Neurolocalization
  • Genetics
<
>
An extremely rare primary degeneration of nervous elements with a range of clinical signs and disease patterns.
Age of Onset: 3-6 months of age
Sex Predisposition: Any sex of animal can be affected ​
Clinical Course:
Clinical signs may worsen over time ​
Clinical Signs:
Posture and Appearance  
Tremor
Thoracic limb extension
Opisthotonos
Stiffness

Movement 
Progression from paraparesis to tetraplegia
Ataxia
Generalized weakness
Incoordination
Drifting to the side
Myotonic spasms

Proprioception  
Knuckling on all limbs
Slow postural reflexes

Cranial Nerves
Reduced menace response
Decreased physiologic nystagmus
Head tilt
Difficulty swallowing
 
Spinal Reflexes  
Absent spinal reflexes in hindlimbs
Reduced spinal reflexes in forelimbs
 
Special Functions (e.g. respiration; urination)  
Urinary incontinence
Respiratory failure

Other 
Increased body temperature​
Diffuse CNS
Suspected autosomal dominant mutation in canine orthologue of glial fibrillary acidic protein (GFAP) gene

For breed specific genetic testing, follow the link below:
https://www.wisdompanel.com/en-us/dog-health-conditions/alexander-disease#:~:text=This%20disease%20is%20autosomal%20recessive,different%20genetic%20or%20clinical%20cause.
To read more about this disease click below:
References
Picture
Contact us:
[email protected]

Privacy Policy
Terms and Conditions​
Cookie Policy
Disclaimer
  • Home
  • Search
  • Methodology
  • Contact