HA - Cerebellar Ataxia/Gordon Setter

Race liée:

Nervous system degeneration

Description:

Cerebellum degeneration leading to slowly progressing loss of motor function

Symptomes:

Progressive loss of coordination, truncal sway, intention tremor, severe gait disturbances

Age d'aparition:

Between 6 months and 4 years old

Fréquence:

Not available

Gène impliqué:

RAB24

Mutation testée:

c.113A>C

Transmission:

Autosomal Recessive

Brevet:

Remarques:

An another DNA test (NCL-D) is available to detect an other form of ataxia in this breed.

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