L-2-hydroxyglutaric aciduria is a genetic disease of the nervous system. The clinical signs are high levels of L-2-hydroxyglutaric acid in urine and plasma, seizures, wobbly gait, ataxia, tremors and muscle stiffness and usually appear from 6 months of age.
Transmission
Autosomal recessive
Breed
American Staffordshire Terrier (Amstaff), Staffordshire Bull Terrier
