Dementia due to Wilson disease (Q99875): Difference between revisions
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| description / pt-br | description / pt-br | ||
Demência devida à doença de Wilson, um transtorno genético caracterizado por deposição de cobre nos gânglios da base e características clínicas de tremor e outros transtornos do movimento. | |||
| description / en | description / en | ||
Dementia due to Wilson disease, a genetic disorder characterised by copper deposition in the basal ganglia and clinical features of tremor and other movement disorders. | |||
Revision as of 16:33, 16 August 2026
Dementia due to Wilson disease, a genetic disorder characterised by copper deposition in the basal ganglia and clinical features of tremor and other movement disorders.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_808983384 |
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| English | Dementia due to Wilson disease |
Dementia due to Wilson disease, a genetic disorder characterised by copper deposition in the basal ganglia and clinical features of tremor and other movement disorders. |
