Abstract
Tauopathies are a group of neurodegenerative diseases characterized by pathological intracellular deposits of the protein tau. Isoform composition, morphology and anatomical distribution of cellular tau-immunoreactivities are defining distinct tauopathies as molecular pathological disease entities. The clinical spectrum of tauopathies includes syndromes with primary motor symptoms and with primary cognitive dysfunction. The traditional syndrome-based classification is currently being complemented by a molecular-pathological classification. While the syndrome-based classification is helpful to select symptomatic therapies, and to generate clinical working hypotheses about underlying etiologies, the molecular-pathological classification is most important for the development and application of molecularly tailored disease-modifying therapies.
| Original language | English |
|---|---|
| Pages (from-to) | 664-668 |
| Number of pages | 5 |
| Journal | Revue Neurologique |
| Volume | 174 |
| Issue number | 9 |
| DOIs | |
| State | Published - Nov 2018 |
Keywords
- Corticobasal degeneration
- Corticobasal syndrome
- Progressive supranuclear palsy
- Richardson's syndrome
- Tauopathies
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