Clinical and Neuroimaging Aspects of Familial Frontotemporal Lobar Degeneration Associated with MAPT and GRN Mutations.

Abstract:

:Numerous kindreds with familial frontotemporal lobar degeneration have been linked to mutations in microtubule-associated protein tau (MAPT) or progranulin (GRN) genes. While there are many similarities in the clinical manifestations and associated neuroimaging findings, there are also distinct differences. In this review, we compare and contrast the demographic/inheritance characteristics, histopathology, pathophysiology, clinical aspects, and key neuroimaging findings between those with MAPT and GRN mutations.

journal_name

Adv Exp Med Biol

authors

Boeve BF,Rosen H

doi

10.1007/978-3-030-51140-1_6

subject

Has Abstract

pub_date

2021-01-01 00:00:00

pages

77-92

eissn

0065-2598

issn

2214-8019

journal_volume

1281

pub_type

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