Neurodegenerative disorders involving deposition of abnormal tau protein isoforms ( TAU PROTEINS) in neurons and glial cells in the brain. Pathological aggregations of tau proteins are associated with mutation of the tau gene on chromosome 17 in patients with ALZHEIMER DISEASE; DEMENTIA; PARKINSONIAN DISORDERS; progressive supranuclear palsy ( SUPRANUCLEAR PALSY, PROGRESSIVE); and corticobasal degeneration (MeSH). Tauopathies are a class of neurodegenerative diseases resulting from the pathological aggregation of tau protein in the human brain. The best known of these illnesses is Alzheimer's disease (AD), where tau protein is deposited within neurons in the form of neurofibrillary tangles (NFTs). They were first described by the eponymous Alois Alzheimer in one of his patients suffering from the disorder. Tangles are formed by hyperphosphorylation of a microtubule-associated protein known as tau, causing it to aggregate in an insoluble form. (These aggregations of hyperphosphorylated tau protein are also referred to as PHF, or "paired helical filaments"). The precise mechanism of tangle formation is not completely understood, and it is still controversial whether tangles are a primary causative factor in the disease or play a more peripheral role. AD is also classified as an amyloidosis because of the presence of senile plaques. The degree of NFT involvement in AD is defined by Braak stages. Braak stages I and II are used when NFT involvement is confined mainly to the transentorhinal region of the brain, stages III and IV when there's also involvement of limbic regions such as the hippocampus, and V and VI when there's extensive neocortical involvement. This should not be confused with the degree of senile plaque involvement, which progresses differently. Other conditions in which neurofibrillary tangles are commonly observed include: Progressive supranuclear palsy although with straight filament rather than PHF tau Dementia pugilistica (chronic traumatic encephalopathy) Frontotemporal dementia and parkinsonism linked to chromosome 17 however without detectable β-amyloid plaques. Lytico-Bodig disease (Parkinson-dementia complex of Guam) Tangle-predominant dementia, with NFTs similar to AD, but without plaques. Tends to appear in the very old. Ganglioglioma and gangliocytoma Meningioangiomatosis Subacute sclerosing panencephalitis As well as lead encephalopathy, tuberous sclerosis, Hallervorden-Spatz disease, and lipofuscinosis In Pick's disease and corticobasal degeneration tau proteins are deposited in the form of inclusion bodies within swollen or "ballooned" neurons. Argyrophilic grain disease (AGD), another type of dementia, is marked by the presence of abundant argyrophilic grains and coiled bodies on microscopic examination of brain tissue. Some consider it to be a type of Alzheimer disease. It may co-exist with other tauopathies such as progressive supranuclear palsy and corticobasal degeneration. Some other tauopathies include: Frontotemporal dementia Frontotemporal lobar degeneration The non-Alzheimer's tauopathies are sometimes grouped together as "Pick's complex". There have been many more subtypes of tauopathy than the two that are included in NIF-Dysfunction. These additional tauopathies should probably be added to ND.

http://purl.obolibrary.org/obo/ND_0000151

There have been many more subtypes of tauopathy than the two that are included in NIF-Dysfunction. These additional tauopathies should probably be added to ND.

Neurodegenerative disorders involving deposition of abnormal tau protein isoforms ( TAU PROTEINS) in neurons and glial cells in the brain. Pathological aggregations of tau proteins are associated with mutation of the tau gene on chromosome 17 in patients with ALZHEIMER DISEASE; DEMENTIA; PARKINSONIAN DISORDERS; progressive supranuclear palsy ( SUPRANUCLEAR PALSY, PROGRESSIVE); and corticobasal degeneration (MeSH).

Tauopathies are a class of neurodegenerative diseases resulting from the pathological aggregation of tau protein in the human brain. The best known of these illnesses is Alzheimer's disease (AD), where tau protein is deposited within neurons in the form of neurofibrillary tangles (NFTs). They were first described by the eponymous Alois Alzheimer in one of his patients suffering from the disorder. Tangles are formed by hyperphosphorylation of a microtubule-associated protein known as tau, causing it to aggregate in an insoluble form. (These aggregations of hyperphosphorylated tau protein are also referred to as PHF, or "paired helical filaments"). The precise mechanism of tangle formation is not completely understood, and it is still controversial whether tangles are a primary causative factor in the disease or play a more peripheral role. AD is also classified as an amyloidosis because of the presence of senile plaques. The degree of NFT involvement in AD is defined by Braak stages. Braak stages I and II are used when NFT involvement is confined mainly to the transentorhinal region of the brain, stages III and IV when there's also involvement of limbic regions such as the hippocampus, and V and VI when there's extensive neocortical involvement. This should not be confused with the degree of senile plaque involvement, which progresses differently. Other conditions in which neurofibrillary tangles are commonly observed include: Progressive supranuclear palsy although with straight filament rather than PHF tau Dementia pugilistica (chronic traumatic encephalopathy) Frontotemporal dementia and parkinsonism linked to chromosome 17 however without detectable β-amyloid plaques. Lytico-Bodig disease (Parkinson-dementia complex of Guam) Tangle-predominant dementia, with NFTs similar to AD, but without plaques. Tends to appear in the very old. Ganglioglioma and gangliocytoma Meningioangiomatosis Subacute sclerosing panencephalitis As well as lead encephalopathy, tuberous sclerosis, Hallervorden-Spatz disease, and lipofuscinosis In Pick's disease and corticobasal degeneration tau proteins are deposited in the form of inclusion bodies within swollen or "ballooned" neurons. Argyrophilic grain disease (AGD), another type of dementia, is marked by the presence of abundant argyrophilic grains and coiled bodies on microscopic examination of brain tissue. Some consider it to be a type of Alzheimer disease. It may co-exist with other tauopathies such as progressive supranuclear palsy and corticobasal degeneration. Some other tauopathies include: Frontotemporal dementia Frontotemporal lobar degeneration The non-Alzheimer's tauopathies are sometimes grouped together as "Pick's complex".

Alexander P. Cox

http://en.wikipedia.org/wiki/Tauopathy

http://neurolex.org/wiki/Category:Tauopathy

http://ontology.neuinfo.org/NIF/Dysfunction/NIF-Dysfunction.owl#birnlex_12696

tauopathy

ND:0000151

tauopathy

http://purl.obolibrary.org/obo/ND_0000113