| Literature DB >> 28247171 |
Vittorio Mantero1, Claudia Tarlarini2, Angelo Aliprandi3, Giuseppe Lauria4, Andrea Rigamonti3, Lucia Abate5, Paola Origone6, Paola Mandich7, Silvana Penco2, Andrea Salmaggi3.
Abstract
Amyotrophic lateral sclerosis (ALS), frontotemporal degeneration and Parkinson's disease may be different expressions of the same neurodegenerative disease. However, association between ALS and parkinsonism-dementia complex (ALS-PDC) has only rarely been reported apart from the cluster detected in Guam. We report a patient presenting with ALS-PDC in whom pathological mutations/expansions were investigated. No other family members were reported to have any symptoms of a neurological condition. Our case demonstrates that ALS-PDC can occur as a sporadic disorder, even though the coexistence of the three clinical features in one patient suggests a single underlying genetic cause. It is known that genetic testing should be preferentially offered to patients with ALS who have affected first or second-degree relatives. However, this case illustrates the importance of genetic counseling for family members of patients with sporadic ALC-PDC in order to provide education on the low recurrence risk. Here, we dicuss the ethical, psychological and practical consequences for patients and their relatives.Entities:
Keywords: Amyotrophic lateral sclerosis; Dementia; Frontotemporal degeneration; Genetic; Genetic counseling; Genetic test; Guam complex; Parkinson disease; Parkinsonism
Mesh:
Year: 2017 PMID: 28247171 DOI: 10.1007/s10897-017-0088-5
Source DB: PubMed Journal: J Genet Couns ISSN: 1059-7700 Impact factor: 2.537