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FTDPS

Frontotemporal dementia and parkinsonism linked to chromosome 17

parkinsonism linked to chromosome 17 (FTDP-17) is an autosomal dominant neurodegenerative tauopathy and Parkinson plus syndrome. FTDP-17 is caused by mutations in

Frontotemporal dementia

Tau-positive frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) is caused by mutations in the MAPT gene on chromosome 17 that encodes

Progressive supranuclear palsy

PSP, corticobasal degeneration, and frontotemporal dementia (especially FTDP-17) to be variations of the same disease. Others consider them separate diseases

Corticobasal degeneration

corticobasal degeneration syndrome (CBDS). Alzheimer's disease, Pick's disease, FTDP-17 and progressive supranuclear palsy can display a corticobasal syndrome

Tauopathy

(CBD) Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) Vacuolar tauopathy Lytico-bodig disease (Parkinson-dementia complex of

Tau protein

M, Spillantini MG (July 2000). "Tau mutations in frontotemporal dementia FTDP-17 and their relevance for Alzheimer's disease". Biochimica et Biophysica

Hereditary diffuse leukoencephalopathy with spheroids

with HDLS that was initially thought to be due to another disease process (FTDP-17), but only an autopsy of one and then other family members revealed it

Splice site mutation

tau protein was found to be correlated with inherited dementia (known as FTDP-17). The splice-site mutations all destabilize a potential stem–loop structure

Li Gan

of neurodegeneration in conditions such as Alzheimer's disease (AD) and FTDP-17. Her lab has also developed induced pluripotent stem cell culture models

Alison Goate

missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17". Nature. 393 (6686): 702–5. doi:10.1038/31508. PMID 9641683.. Gitcho