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Descriptor English: Frontotemporal Dementia
Descriptor Spanish: Demencia Frontotemporal
Descriptor demencia frontotemporal
Scope note: La forma clínica más frecuente de DEGENERACIÓN DEL LÓBULO FRONTOTEMPORAL que se presenta con cambios de la personalidad y del comportamiento, con frecuencia asociados a desinhibición, apatía y anosognosia.
Descriptor Portuguese: Demência Frontotemporal
Descriptor French: Démence frontotemporale
Entry term(s): Complex, Disinhibition-Dementia-Parkinsonism-Amyotrophy
Complex, Disinhibition-Dementia-Parkinsonism-Amytrophy
Complices, Disinhibition-Dementia-Parkinsonism-Amyotrophy
Complices, Disinhibition-Dementia-Parkinsonism-Amytrophy
DDPAC
Dementia, Frontotemporal
Dementia, Frontotemporal Lobe
Dementia, Frontotemporal Lobe (FLDEM)
Dementia, Frontotemporal, with Parkinsonism
Dementia, GRN-Related Frontotemporal
Dementia, Hereditary Dysphasic Disinhibition
Dementia, Semantic
Dementia, Ubiquitin-Positive Frontotemporal
Dementias, Frontotemporal
Dementias, Frontotemporal Lobe
Dementias, Frontotemporal Lobe (FLDEM)
Dementias, GRN-Related Frontotemporal
Dementias, Semantic
Dementias, Ubiquitin-Positive Frontotemporal
Disease, Familial Pick's
Disease, Wilhelmsen-Lynch
Diseases, Familial Pick's
Diseases, Wilhelmsen-Lynch
Disinhibition Dementia Parkinsonism Amyotrophy Complex
Disinhibition Dementia Parkinsonism Amytrophy Complex
Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex
Disinhibition-Dementia-Parkinsonism-Amyotrophy Complices
Disinhibition-Dementia-Parkinsonism-Amytrophy Complex
Disinhibition-Dementia-Parkinsonism-Amytrophy Complices
FTD-GRN
FTD-PGRN
FTDP-17
FTLD with TDP 43 Pathology
FTLD with TDP-43 Pathology
FTLD-17 GRN
FTLD-TDP
Familial Pick Disease
Familial Pick's Disease
Familial Pick's Diseases
Familial Picks Disease
Frontotemporal Dementia with Parkinsonism
Frontotemporal Dementia with Parkinsonism 17
Frontotemporal Dementia with Parkinsonism-17
Frontotemporal Dementia, GRN-Related
Frontotemporal Dementia, Ubiquitin Positive
Frontotemporal Dementia, Ubiquitin-Positive
Frontotemporal Dementias
Frontotemporal Dementias, GRN-Related
Frontotemporal Dementias, Ubiquitin-Positive
Frontotemporal Lobar Degeneration With Ubiquitin Positive Inclusions
Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions
Frontotemporal Lobe Dementia
Frontotemporal Lobe Dementia (FLDEM)
Frontotemporal Lobe Dementias
Frontotemporal Lobe Dementias (FLDEM)
GRN Related Frontotemporal Dementia
GRN-Related Frontotemporal Dementia
GRN-Related Frontotemporal Dementias
HDDD1
HDDD2
Hereditary Dysphasic Disinhibition Dementia
Lobe Dementia, Frontotemporal
Lobe Dementias, Frontotemporal
Multiple System Tauopathy with Presenile Dementia
Pick's Disease, Familial
Pick's Diseases, Familial
Semantic Dementia
Semantic Dementias
Ubiquitin-Positive Frontotemporal Dementia
Ubiquitin-Positive Frontotemporal Dementias
Wilhelmsen Lynch Disease
Wilhelmsen-Lynch Disease
Wilhelmsen-Lynch Diseases
Tree number(s): C10.228.140.380.266.299
C10.574.950.300.299
C18.452.845.800.300.299
F03.615.400.380.299
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D057180
Scope note: 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.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
SU surgery
TH therapy
UR urine
VI virology
Previous Indexing: Dementia (1994-2009)
Public MeSH Note: 2010
History Note: 2010
DeCS ID: 53512
Unique ID: D057180
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2010/01/01
Date of Entry: 2009/07/06
Revision Date: 2015/06/23
Frontotemporal Dementia - Preferred
Concept UI M0534991
Scope note 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.
Preferred term Frontotemporal Dementia
Entry term(s) Complex, Disinhibition-Dementia-Parkinsonism-Amyotrophy
Complex, Disinhibition-Dementia-Parkinsonism-Amytrophy
Complices, Disinhibition-Dementia-Parkinsonism-Amyotrophy
Complices, Disinhibition-Dementia-Parkinsonism-Amytrophy
DDPAC
Dementia, Frontotemporal
Dementia, Frontotemporal Lobe
Dementia, Frontotemporal Lobe (FLDEM)
Dementia, Frontotemporal, with Parkinsonism
Dementia, GRN-Related Frontotemporal
Dementia, Hereditary Dysphasic Disinhibition
Dementia, Ubiquitin-Positive Frontotemporal
Dementias, Frontotemporal
Dementias, Frontotemporal Lobe
Dementias, Frontotemporal Lobe (FLDEM)
Dementias, GRN-Related Frontotemporal
Dementias, Ubiquitin-Positive Frontotemporal
Disease, Familial Pick's
Disease, Wilhelmsen-Lynch
Diseases, Familial Pick's
Diseases, Wilhelmsen-Lynch
Disinhibition Dementia Parkinsonism Amyotrophy Complex
Disinhibition Dementia Parkinsonism Amytrophy Complex
Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex
Disinhibition-Dementia-Parkinsonism-Amyotrophy Complices
Disinhibition-Dementia-Parkinsonism-Amytrophy Complex
Disinhibition-Dementia-Parkinsonism-Amytrophy Complices
FTD-GRN
FTD-PGRN
FTDP-17
FTLD with TDP 43 Pathology
FTLD with TDP-43 Pathology
FTLD-17 GRN
FTLD-TDP
Familial Pick Disease
Familial Pick's Disease
Familial Pick's Diseases
Familial Picks Disease
Frontotemporal Dementia with Parkinsonism
Frontotemporal Dementia with Parkinsonism 17
Frontotemporal Dementia with Parkinsonism-17
Frontotemporal Dementia, GRN-Related
Frontotemporal Dementia, Ubiquitin Positive
Frontotemporal Dementia, Ubiquitin-Positive
Frontotemporal Dementias
Frontotemporal Dementias, GRN-Related
Frontotemporal Dementias, Ubiquitin-Positive
Frontotemporal Lobar Degeneration With Ubiquitin Positive Inclusions
Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions
Frontotemporal Lobe Dementia
Frontotemporal Lobe Dementia (FLDEM)
Frontotemporal Lobe Dementias
Frontotemporal Lobe Dementias (FLDEM)
GRN Related Frontotemporal Dementia
GRN-Related Frontotemporal Dementia
GRN-Related Frontotemporal Dementias
HDDD1
HDDD2
Hereditary Dysphasic Disinhibition Dementia
Lobe Dementia, Frontotemporal
Lobe Dementias, Frontotemporal
Multiple System Tauopathy with Presenile Dementia
Pick's Disease, Familial
Pick's Diseases, Familial
Ubiquitin-Positive Frontotemporal Dementia
Ubiquitin-Positive Frontotemporal Dementias
Wilhelmsen Lynch Disease
Wilhelmsen-Lynch Disease
Wilhelmsen-Lynch Diseases
Semantic Dementia - Narrower
Concept UI M0334717
Preferred term Semantic Dementia
Entry term(s) Dementia, Semantic
Dementias, Semantic
Semantic Dementias



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