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hereditary cerebellar ataxia

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hereditary cerebellar ataxia
n.
A disease of later childhood and early adult life marked by ataxic gait, hesitating and explosive speech, nystagmus, and sometimes optic neuritis.

hereditary cerebellar ataxia
AAA syndrome An AR condition characterized by cerebellar ataxia, degeneration of esophageal myenteric ganglion cells, and achalasia


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The shaker mutant rat, originally present in Sprague Dailey outbred stock, is an excellent animal model for anatomical and movement analysis studies of hereditary cerebellar ataxia.
Once the gait analysis is complete, we will be able to say with greater precision when affected dogs first begin showing clinical signs With the preliminary data generated in these studies, we applied for and received a 3 year NIH grant to continue exploring the X-linked canine ataxia as a model of human hereditary cerebellar ataxia.
 
 
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