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... > Nervous System Diseases > Central Nervous System Diseases > Brain Diseases > Dementia > Frontotemporal Lobar Degeneration > Frontotemporal Dementia
Mental Disorders > Neurocognitive Disorders > Dementia > Frontotemporal Lobar Degeneration > Frontotemporal Dementia
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Proteostasis Deficiencies > TDP-43 Proteinopathies > Frontotemporal Lobar Degeneration > Frontotemporal Dementia
Nervous System Diseases > Neurodegenerative Diseases > TDP-43 Proteinopathies > Frontotemporal Lobar Degeneration > Frontotemporal Dementia

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Frontotemporal Dementia  

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Tipo

  • mesh:Descriptor

Definición

  • The most common clinical form of FRONTOTEMPORAL LOBAR DEGENERATION, this dementia presents with personality and behavioral changes often associated with disinhibition, apathy, and lack of insight.

Concepto genérico

Conceptos específicos

Etiquetas alternativas

  • DDPAC
  • Dementia, Frontotemporal
  • Dementia, Frontotemporal, with Parkinsonism
  • Dementia, Hereditary Dysphasic Disinhibition
  • Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex
  • Disinhibition-Dementia-Parkinsonism-Amytrophy Complex
  • Familial Pick's Disease
  • Frontotemporal Dementia, Ubiquitin-Positive
  • Frontotemporal Dementia with Parkinsonism
  • Frontotemporal Dementia with Parkinsonism-17
  • Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions
  • Frontotemporal Lobe Dementia
  • Frontotemporal Lobe Dementia (FLDEM)
  • FTD-GRN
  • FTDP-17
  • FTD-PGRN
  • FTLD with TDP-43 Pathology
  • FTLD-17 GRN
  • FTLD-TDP
  • GRN-Related Frontotemporal Dementia
  • HDDD1
  • HDDD2
  • Hereditary Dysphasic Disinhibition Dementia
  • Multiple System Tauopathy with Presenile Dementia
  • Wilhelmsen-Lynch Disease

En otras lenguas

  • Démence frontotemporale

    francés

  • Démence fronto-temporale
  • Démence frontotemporale avec parkinsonisme liée au chromosome 17
  • DFT (Démence FrontoTemporale)
  • DFTP-17

URI

http://data.loterre.fr/ark:/67375/JVR-R57TC261-1

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