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Marie's ataxia |
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Marie's ataxia [mə′rēz ā′tak·sē·ə] (medicine) A hereditary ataxia combining features of cerebellar, posterior column, and pyramidal tract lesions, with onset after age 20, normal or exaggerated deep tendon reflexes, and frequently optic atrophy and oculomotor palsies, but no clubfeet or scoliosis. How to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit webmaster's page for free fun content. |
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