VNDD
  • Home
  • Search
  • Methodology
  • Contact
<Return to Disease List
Mitochondrial (Fission) Encephalopathy
  • Description
  • Signalment
  • Clinical Features
  • Neurolocalization
  • Genetics
<
>
Mitochondrial encephalopathy is caused by abnormal mitochondrial function/metabolism. Organs that are most dependent on oxidative metabolism are most severely affected.
Age of Onset: 6 months - 6 years of age
Sex Predisposition: Any sex of animal can be affected
Clinical Course:
​Clinical signs may progress
Clinical Signs:
Behavioral/Mental Awareness
Behavior abnormalities
Seizures

Posture and Appearance
Head tilt
Head tremor
Extensor rigidity of thoracic limbs
Wide based stance

Movement
Ataxia
Hypermetric gait
Loss of balance
Spastic tetraparesis
Weakness

Cranial Nerves
Absent menace response
Nystagmus
Visual defects

Pain Sensation
Facial hypalgesia
Intracranial
Suspected autosomal recessive inheritance of in-frame deletion in canine PITRM1 gene
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