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Frontotemporal Lobar Degeneration  

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Tipo

  • mesh:Descriptor

Definición

  • Heterogeneous group of neurodegenerative disorders characterized by frontal and temporal lobe atrophy associated with neuronal loss, gliosis, and dementia. Patients exhibit progressive changes in social, behavioral, and/or language function. Multiple subtypes or forms are recognized based on presence or absence of TAU PROTEIN inclusions. FTLD includes three clinical syndromes: FRONTOTEMPORAL DEMENTIA, semantic dementia, and PRIMARY PROGRESSIVE NONFLUENT APHASIA.

Etiquetas alternativas

  • FTLD

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-HGM03894-L

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