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Hereditary diseases of cats

CSD002
Gangliosidosis GM2, type II, Burmese cats
GM2
5
Cats
Sandhoff disease
Some breeds
Australian labradoodle
Hereditary diseases
Progressive neuronopathic lysosomal storage disease caused by a deficiency in b-N-acetylhexosaminidase activity. Gangliosidosis GM2 can have varying degrees of severity. Kittens begin to show the characteristic signs of cerebellar dysfunction at about 2 months of age. By 4 months, other neurological signs gradually appear and subsequently sick kittens die at about 7 months of age. Magnetic resonance imaging shows an enlarged ventricular system, T1 hyperintensity in the inner capsule and T2 hyperintensity in the white matter of the brain.
Autosomal recessive inheritance
HEXB
N
M