GRN-related frontotemporal lobar degeneration with Tdp43 inclusions

MONDO:0011842

A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has material basis in mutation in the GRN gene on chromosome 17q21.31.

Also known as: FTLD-TDP, GRN-related, aphasia, primary progressive, dementia, hereditary dysphasic disinhibition, frontotemporal dementia with TDP43 inclusions, GRN-related, frontotemporal dementia, ubiquitin-positive, frontotemporal lobar degeneration with TDP43 inclusions, GRN-related, frontotemporal lobar degeneration with ubiquitin-positive inclusions

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