Frontotemporal dementia
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 (see these terms).
Cell Lines
- ICGi052-A
- ICGi052-B
- ICGi052-B-1
- ICGi052-B-2
- ICNDXHi001-A
- JUCGRMi007-A
- JUCGRMi007-B
- JUCGRMi007-C
- SIGi001-A-16
- LUBi001-A
- LUBi001-B
- LUBi001-C
- SIGi001-A-12
- SIGi001-A-3
- SIGi001-A-4
- SIGi001-A-5
- SIGi001-A-6
- SIGi001-A-7
- UCLi001-A
- UCLi002-A
- UCLi003-A
- UCLi004-A
- UCLi004-B
- UCLi004-C
- UCLi009-A
- UCLi009-B
- UCLi010-A
- UCLi010-B
Link
For more information, please consult the corresponding entry in Orphanet* .
*Orphanet: an online rare disease and orphan drug data base. Copyright, INSERM 1999. Available on http://www.orpha.net.