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Up to: Frontotemporal dementia · Primary progressive aphasia
GRN-related frontotemporal lobar degeneration with Tdp43 inclusions
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.
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Progressive non-fluent aphasia 23 trials · 44 incl. sub-types Sub-types →