Dementia due to Fragile X Syndrome (Q99872): Difference between revisions
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Latest revision as of 16:33, 16 August 2026
Dementia due to Fragile X Syndrome, a rare genetic syndrome characterised by intention tremor, ataxia, parkinsonism, cognitive and behavioural changes. It is an inclusion body disease with intranuclear inclusions throughout the brain, particularly in the hippocampus and frontal cortex, as well as in the deep cerebellar nuclei. Some have characterised the dementia as one of frontal subcortical subtype.
| Language | Label | Description | Also known as |
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| default for all languages | ID_874230470 |
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| English | Dementia due to Fragile X Syndrome |
Dementia due to Fragile X Syndrome, a rare genetic syndrome characterised by intention tremor, ataxia, parkinsonism, cognitive and behavioural changes. It is an inclusion body disease with intranuclear inclusions throughout the brain, particularly in the hippocampus and frontal cortex, as well as in the deep cerebellar nuclei. Some have characterised the dementia as one of frontal subcortical subtype. |
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CID11:ID_874230470
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dki-india-ID_874230470
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Concluído
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15 August 2026
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