olivopontocerebellar degeneration

olivopontocerebellar degeneration
see under atrophy.

Medical dictionary. 2011.

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  • olivopontocerebellar atrophy — ol·i·vo·pon·to·cer·e·bel·lar atrophy .pän tō .ser ə bel ər n an inherited disease esp. of mid to late life that is characterized by ataxia, hypotonia, dysarthria, and degeneration of the cerebellar cortex, middle cerebellar peduncles, and… …   Medical dictionary

  • Olivopontocerebellar atrophy — Classification and external resources Sagittal section through right cerebellar hemisphere. The right olive has also been cut sagitally. ICD 10 G …   Wikipedia

  • degeneration — 1. Deterioration; passing from a higher to a lower level or type. 2. A worsening of mental, physical, or moral qualities. 3. A retrogressive pathologic change in cells or tissues, in consequence of which their functions are often impaired or… …   Medical dictionary

  • OPCD — olivopontocerebellar degeneration …   Medical dictionary

  • OPCD — • olivopontocerebellar degeneration …   Dictionary of medical acronyms & abbreviations

  • Atrophy — Wasting away or diminution. Muscle atrophy is wasting of muscle, decrease in muscle mass. A nerve can also show atrophy. For example, atrophy of the optic nerve diminishes vision. * * * A wasting of tissues, organs, or the entire body, as from… …   Medical dictionary

  • multiple system atrophy — (MSA), multisystem atrophy a progressive neurodegenerative disorder characterized by striatonigral and olivopontocerebellar degeneration with formation of Papp Lantos bodies and exhibiting varying combinations of parkinsonism, cerebellar ataxia,… …   Medical dictionary

  • List of anatomical topics — This page aims to list articles related to anatomy. This list is not necessarily complete or up to date if you see an article that should be here but isn t (or one that shouldn t be here but is), please update the page accordingly. NOTOC A… …   Wikipedia

  • Multiple system atrophy — Classification and external resources ICD 10 G90.3 ICD 9 333.0 …   Wikipedia

  • Spinocerebellar ataxia — (SCA) is a genetic disease with multiple types, each of which could be considered a disease in its own right. ymptomsSpinocerebellar ataxia (SCA) is one of a group of genetic disorders characterized by slowly progressive incoordination of gait… …   Wikipedia

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