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Autosomal recessive cerebellar ataxia
・ Autosomal recessive multiple epiphyseal dysplasia
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Autosomal recessive cerebellar ataxia : ウィキペディア英語版
Autosomal recessive cerebellar ataxia
Autosomal recessive cerebellar ataxia type 1 (ARCA1) is a condition characterized by progressive problems with movement. Signs and symptoms of the disorder first appear in early to mid-adulthood. People with this condition initially experience impaired speech (dysarthria), problems with coordination and balance (ataxia), or both. They may also have difficulty with movements that involve judging distance or scale (dysmetria). Other features of ARCA1 include abnormal eye movements (nystagmus) and problems following the movements of objects with their eyes. The movement problems are slowly progressive, often resulting in the need for a cane, walker, or wheelchair.〔(【引用サイトリンク】url=http://ghr.nlm.nih.gov/condition/autosomal-recessive-cerebellar-ataxia-type-1 )
==Types of ARCA ==


抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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