INVESTIGADORES
ALLEGRI Ricardo F.
artículos
Título:
Familial dementia with frontotemporal features associated with Met146Val presenilin-1 mutation
Autor/es:
RIUDAVETS MA, BARTOLONI L, TRONCOSO JC, PLETNIKOVA O, ST GEORGE-HYSLOP P, SCHULTZ M, SEVLEVER G, ALLEGRI RF.
Revista:
BRAIN PATHOLOGY
Editorial:
WILEY-BLACKWELL PUBLISHING, INC
Referencias:
Lugar: Londres; Año: 2013 vol. 23 p. 595 - 600
ISSN:
1015-6305
Resumen:
Most of the mutations in the presenilin-1 gene (PS-1) are associated with familial Alzheimer?s disease (AD). However, certain examples can be associated with frontotemporal dementia (FTD). We performed a clinical evaluation of individuals belonging to a family with the FTD phenotype, and additional molecular studies and neuropathological assessment of the proband. The PS-1 M146V mutation was found in the 50-year-old subject (the proband) with family history of early-onset FTD. Neuropathological examination showed abundant amyloid plaques, widespread neurofibrillary pathology, Pick bodies in the hippocampus and cortex, cortical globose tangles and ubiquitin-positive nuclear inclusions in white matter oligodendrocytes. We report a kindred with clinical features of FTD, whose proband bore the PS-1 M146V mutation and showed diffuse Alzheimer?s type pathology and Pick bodies on post-mortem neuropathological examination. As with other mutations within the same codon, this substitution may predispose to both diseases by affecting APP and/or tau processing.