Structured Summary
Abstract
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.
MeSH Record
Classification
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MeSH Record
Synonyms
7 entry terms
- FTLD
- Degeneration, Frontotemporal Lobar
- Degenerations, Frontotemporal Lobar
- FTLDs
- Frontotemporal Lobar Degenerations
- Lobar Degeneration, Frontotemporal
- Lobar Degenerations, Frontotemporal
MeSH Record
Aspects Covered
31 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, rehabilitation, surgery, therapy, urine, virology.
MeSH Record
History Note
2010; use DEMENTIA 2000-2009; for SEMANTIC DEMENTIA use DEMENTIA 2000-2009
MeSH Record
Previous Indexing
- Dementia (2002-2009)
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AMA Style
References
- National Library of Medicine. Frontotemporal Lobar Degeneration. Medical Subject Headings (MeSH). 2026. Unique ID D057174. http://id.nlm.nih.gov/mesh/2026/D057174
- Frontotemporal Lobar Degeneration. In: Wikipedia. https://en.wikipedia.org/wiki/Frontotemporal_lobar_degeneration
- Frontotemporal Lobar Degeneration. In: Wikidata. https://www.wikidata.org/wiki/Q18579