|
sporadic: olivopontocerebellar atrophy or degeneration,
olivocerebellar atrophy or degeneration,
Multisystem atrophy (MSA),
ataxia
Marie's ataxia,
Holmes ataxia ,
Menzel's ataxia,
ataxia with parkinsonism, autonomic neuropathy,
corticospinal features or dementia
spastic ataxia, etc. |
hereditary:
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. |
