Frontotemporal dementia due to C9orf72 mutation (Q99482): Difference between revisions

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Revision as of 16:08, 16 August 2026

TD due to mutation in open reading frame 72 of chromosome 9. Clinically it can present as FTD (specifically behavioural variant), motor neuron disease, or FTD with motor neuron disease.
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ID_214328399
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    Frontotemporal dementia due to C9orf72 mutation
    TD due to mutation in open reading frame 72 of chromosome 9. Clinically it can present as FTD (specifically behavioural variant), motor neuron disease, or FTD with motor neuron disease.

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      CID11:ID_214328399
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