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The Genetics of Monogenic Frontotemporal Dementia

1 Sept 2015

Abstract excerpt

ABSTRACT Around 10-15% of patients diagnosed with frontotemporal dementia (FTD) have a positive family history for FTD with an autosomal dominant pattern of inheritance. Since the identification of mutations in MAPT(microtubuleassociated protein tau gene) in 1998, over 10 other genes have been associated with FTD spectrum disorders, discussed in this review. Along with MAPT, mutations in GRN(progranulin) and...

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PMID: 29213965
DOI: 10.1590/1980-57642015dn93000003

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