| Literature DB >> 24169076 |
Nicola Ticozzi1, Cinzia Tiloca2, Daniela Calini3, Stella Gagliardi4, Alessandra Altieri3, Claudia Colombrita5, Cristina Cereda4, Antonia Ratti5, Gianni Pezzoli6, Barbara Borroni7, Stefano Goldwurm6, Alessandro Padovani7, Vincenzo Silani5.
Abstract
Expansion of a GGGGCC repeat (RE) in the C9orf72 gene has been recently reported as the main genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Given the growing evidence of genetic and clinicopathologic overlap among ALS, FTD, and other neurodegenerative diseases, we investigated the occurrence of RE in a subset of 9 patients with ALS-plus syndromes, including Parkinson's disease (PD), progressive supranuclear palsy (PSP), corticobasal syndrome (CBS), and multiple system atrophy. We identified RE in 2 ALS-plus individuals (22.2%) displaying PSP and CBS features. On the basis of this finding, we extended our analysis to a cohort composed of 190 PD, 103 CBS, 107 PSP, and 177 Alzheimer's disease cases. We did not identify any RE in these patients, indicating that C9orf72 is in all probability not involved in the pathogenesis of these disorders. However, the high frequency of C9orf72 RE in patients with ALS-plus syndromes suggests that, similar to ALS-FTD patients, individuals with combined motor neuron and extrapyramidal features should be screened for RE, independent of their family history.Entities:
Keywords: Amyotrophic lateral sclerosis; C9orf72; Corticobasal syndrome; Frontotemporal lobar degeneration; Neurogenetics; Progressive supranuclear palsy
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Year: 2013 PMID: 24169076 DOI: 10.1016/j.neurobiolaging.2013.09.037
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673