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

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15 August 2026
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Latest 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
    English
    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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      dki-india-ID_214328399
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      Concluído
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      15 August 2026
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