FTD with tau-positive inclusions: This includes classic Pick’s disease, Progressive Supranuclear Palsy, Corticobasal degeneration, argyrophilic grain disease, and patients with mutation of the Microtubule-associated protein tau (MAPT) gene on chromosome 17 (FTDP-17).[71]. This evidence concerns the gene MAPT and argyrophilic grain disease.