| Literature DB >> 32483606 |
Karina Chornenka1, Veronica Hirsch-Reinshagen2, Mari Perez-Rosendahl3, Howard Feldman4, Freddi Segal-Gidan5, Harry V Vinters6,7, Ian R Mackenzie2.
Abstract
Atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions (aFTLD-U) is an uncommon cause of frontotemporal dementia characterized by fused in sarcoma-positive inclusions. It is classified as a subtype of frontotemporal lobar degeneration with FUS pathology. Cases with aFTLD-U pathology typically display an early onset of symptoms and severe psychobehavioral changes in the absence of significant aphasia, cognitive-intellectual dysfunction or motor features. This phenotype is regarded as being sufficiently unusual and consistent as to allow antemortem diagnosis with a high degree of accuracy. In this report, we describe 2 cases with aFTLD-U pathology that broaden the associated phenotype to include later age of onset, milder behavioral abnormalities and early memory and language impairment.Entities:
Keywords: FTLD-FUS; Frontotemporal dementia; Frontotemporal lobar degeneration; Fused in sarcoma; aFTLD-U
Year: 2020 PMID: 32483606 DOI: 10.1093/jnen/nlaa045
Source DB: PubMed Journal: J Neuropathol Exp Neurol ISSN: 0022-3069 Impact factor: 3.685