Autosomal recessive cerebellar ataxia type 1 is a condition identified by progressive troubles with movement because of a loss of nerve cells in the part of the brain that collaborates movement. Signs and symptoms of the disorder first appear in very early to mid-adulthood. People with this problem initially experience impaired speech, troubles with coordination and equilibrium, or both. Other features of ARCA1 include abnormal eye movements and problems following the activities of things with the eyes.
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