- cerebral atrophy
- церебральная атрофия
English-Russian small dictionary of medicine. Г.Ю. Бельман, А.Е. Бойков.. 2015.
English-Russian small dictionary of medicine. Г.Ю. Бельман, А.Е. Бойков.. 2015.
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