Literature DB >> 32483606

Expanding the Phenotype of Frontotemporal Lobar Degeneration With FUS-Positive Pathology (FTLD-FUS).

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.
© 2020 American Association of Neuropathologists, Inc. All rights reserved.

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


  1 in total

1.  A Case of Frontotemporal Lobar Degeneration With FUS-Positive Pathology (FTLD-FET) With Corticobasal Features and Language Deficits.

Authors:  Vanessa Goodwill; David Coughlin; Donald Pizzo; Douglas Galasko; Lawrence A Hansen; Shauna H Yuan; Annie Hiniker
Journal:  J Neuropathol Exp Neurol       Date:  2021-09-27       Impact factor: 3.685

  1 in total

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