Gerstmann syndrome (Q47114): Difference between revisions
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A síndrome de Gerstmann é um transtorno neurológico muito raro caracterizado pela associação específica de acalculia, agnosia digital, desorientação esquerda-direita e agrafia, sendo supostamente secundária a um dano focal subcortical na substância branca no lobo parietal. | |||
| description / en | description / en | ||
Gerstmann syndrome is a very rare neurological disorder characterised by the specific association of acalculia, finger agnosia, left-right disorientation, and agraphia, which is supposed to be secondary to a focal subcortical white matter damage in the parietal lobe. | |||
Revision as of 16:05, 13 August 2026
Gerstmann syndrome is a very rare neurological disorder characterised by the specific association of acalculia, finger agnosia, left-right disorientation, and agraphia, which is supposed to be secondary to a focal subcortical white matter damage in the parietal lobe.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | MB4C |
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| English | Gerstmann syndrome |
Gerstmann syndrome is a very rare neurological disorder characterised by the specific association of acalculia, finger agnosia, left-right disorientation, and agraphia, which is supposed to be secondary to a focal subcortical white matter damage in the parietal lobe. |
