| Literature DB >> 24718101 |
Silvia Testi1, Silvio Peluso2, Gian Maria Fabrizi1, Antonella Antenora2, Cinzia Valeria Russo2, Sabina Pappatà3, Alessandro Padovani4, Moreno Ferrarini1, Alessandro Filla2.
Abstract
PSEN1 gene mutations represent the first cause of familiar early-onset Alzheimer's disease (EOAD). More than 190 mutations in PSEN1 have been reported to date. The clinical phenotype is mainly characterized by cognitive decline but movement disorders have been rarely described. We report a novel PSEN1 mutation (p.Thr147Pro) responsible for a sporadic early-onset dementia with prominent cerebellar symptoms, resembling a spinocerebellar syndrome. Neuroradiological and cerebrospinal fluid biomarkers examinations were performed on the patient, showing typical findings of EOAD and suggesting the pathogenicity of the novel mutation. Our study widens the number of unusual phenotypes related to PSEN1 mutations.Entities:
Keywords: Ataxia; dominantly-inherited spinocerebellar ataxias; early onset Alzheimer's disease; human PSEN1 protein
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Year: 2014 PMID: 24718101 DOI: 10.3233/JAD-140081
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472