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frontotemporal dementia, right temporal atrophy variant (RTLA) - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

frontotemporal dementia, right temporal atrophy variant

MONDO:0017399

Also known as:RTLArvFTD

Overview

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.

Diagnosis

Biomarker and diagnostic research for frontotemporal dementia, right temporal atrophy variant has been reported in the published literature.

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for frontotemporal dementia, right temporal atrophy variant.

38 publications have been identified in PubMed for frontotemporal dementia, right temporal atrophy variant. Research spans Basic Science / Preclinical (47%), Case Report / Case Series (21%), and Diagnostic / Biomarker (16%).

Research Type	Count	% of Total
Laboratory research	18	47%

Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 11:21 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:293848

Questions for Your Care Team

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frontotemporal dementia, right temporal atrophy variant

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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