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Metabolic Encephalopathy (Succinic Semialdehyde Dehydrogenase Deficiency) 
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  • Description
  • Signalment
  • Clinical Features
  • Neurolocalization
  • Genetics
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Metabolic encephalopathy caused by succinic semialdehyde dehydrogenase deficiency results in the malfunction of the GABA (neurotransmitter) metabolic pathway, causing neurologic dysfunction.​
Age of Onset: Less than 10 weeks of age
Sex Predisposition: Any sex of animal can be affected
Clinical Course:
​Clinical signs may worsen over time or remain stable after onset
Clinical Signs:
Behavioral/Mental Awareness
Abnormal vocalization 
Altered behavior
Difficult being aroused from sleep
Seizures

Movement
Mild generalized ataxia
Thoracic limb hypermetria

Proprioception
Delayed proprioception in all four limbs

Cranial Nerves
Absent menace response​
Multifocal central nervous system (bilaterally symmetrical lesions of the cerebrum, brainstem, and cerebellum predominantly affecting the grey matter)
Homozygous missense variant in ALDH5A1

For breed specific genetic testing, click the link(s) below:
vgl.ucdavis.edu/test/saluki_enchephalopathy

​www.genomia.cz/en/test/ssadhd/
To read more about this disease click below:
References
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