frontotemporal dementia
MONDO:0017276Also known as: FTD, MSTD, frontotemporal lobe dementia (FLDEM)
- MONDO:
- MONDO:0017276
- Orphanet:
- 282 ↗
Rare disease35 associated genes
Description
Frontotemporal dementia (FTD) comprises a group of neurodegenerative disorders, characterized by progressive changes in behavior, executive dysfunction and language impairment, as a result of degeneration of the medial prefrontal and frontoinsular cortices. Four clinical subtypes have been identified: semantic dementia, progressive non-fluent aphasia, behavioral variant FTD and right temporal lobar atrophy.
Associated genes
+25 more genes — install the extension to see the full list inline on any page.