Frontotemporal dementia, right temporal atrophy variant

MONDO:0017399

Right temporal lobar atrophy (RTLA) is an anatomic variant of frontotemporal dementia (FTD), characterized by behavioral dysfunction, personality changes, episodic memory loss, and prosopagnosia; attributable to an asymmetrical predominantly right-sided, frontotemporal atrophy.

Also known as: RTLA, rvFTD

173 clinical trials for this condition and its sub-types.

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