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Visit the OPCA Awareness Website to learn more about these diseases! << Please Join/Register for the forum to see the discussion boards >> This forum originally focused on OPCA, Olivopontocerebellar atrophy. This refers to a group of ataxias (listed below) characterized by progressive neurological degeneration affecting the cerebellum, the pons and the inferior olives (all parts of the brain). However, we welcome everyone with any type of Ataxia to this forum! |
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| sporadic ataxias: olivopontocerebellar atrophy or degeneration, olivocerebellar atrophy or degeneration, Multisystem atrophy (MSA), Marie's ataxia, Holmes ataxia, Menzel's ataxia, ataxia with parkinsonism, autonomic neuropathy, corticospinal features or dementia spastic ataxia, etc. | hereditary ataxias: olivopontocerebellar atrophy, spinocerebellar ataxia (SCA), SCA #, "slow-eye movement" ataxia, Machado-Joseph disease, "pure" cerebellar ataxia, OPCA #, ataxia with ophthalmoplegia, ataxia with retinopathy, Marie's ataxia, Holmes ataxia, Menzel's ataxia, spinopontine atrophy, etc. |
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