GRN-related frontotemporal lobar degeneration with Tdp43 inclusions
MONDO:0011842A 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
51 clinical trials for this condition and its sub-types, 6 tagged with GRN-related frontotemporal lobar degeneration with Tdp43 inclusions itself.
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Browse by category →Sub-types of GRN-related frontotemporal lobar degeneration with Tdp43 inclusions
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Progressive non-fluent aphasia 24 trials · 44 incl. sub-types
1 sub-type
- Semantic dementia 32 trials Sub-types →