cerebral atrophy

cerebral atrophy
церебральная атрофия

English-Russian small dictionary of medicine. . 2015.

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  • Cerebral atrophy — Cerebral degeneration Classification and external resources ICD 9 331.9 Cerebral atrophy is a common feature of many of the diseases that affect the brain. Atrophy of any tissue means loss of cells. In brain tissue, atrophy describes a loss of… …   Wikipedia

  • Cerebral palsy — Classification and external resources …   Wikipedia

  • circumscribed cerebral atrophy — Pick disease (def. 1) …   Medical dictionary

  • 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

  • Cerebral calcification, nonarteriosclerotic — This syndrome described in 1930 by T. Fahr is a genetic (inherited) neurological disorder characterized by abnormal deposits of calcium in certain of areas of the brain (including the basal ganglia and the cerebral cortex). Symptoms may include… …   Medical dictionary

  • Spinal muscular atrophy — Classification and external resources ICD 10 G12 ICD 9 335.0 …   Wikipedia

  • Dentatorubral-pallidoluysian atrophy — Classification and external resources OMIM 125370 DiseasesDB 32909 MeSH …   Wikipedia

  • Progressive muscular atrophy — Classification and external resources ICD 9 335.21 DiseasesDB 29149 …   Wikipedia

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

  • Autosomal recessive distal spinal muscular atrophy 1 — Classification and external resources OMIM 604320 Autosomal recessive distal spinal muscular atrophy 1 (or spinal muscular atrophy with respiratory distress type 1, or distal spinal muscular atrophy 1)[1] …   Wikipedia

  • Calcification, nonarteriosclerotic cerebral — This condition described in 1930 by T. Fahr (and therefore called Fahr syndrome) is a genetic (inherited) neurological disorder characterized by abnormal deposits of calcium in certain of areas of the brain (including the basal ganglia and the… …   Medical dictionary


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