Abstract
Multiple system atrophy (MSA) is by nature a 'sporadic' disease with no evidence of familial aggregation observed. However, the α-synuclein locus (SNCA) multiplication families have clinically displayed parkinsonism and autonomic dysfunction. The present study did not find any SNCA multiplications in a series of 58 pathologically confirmed MSA cases excluding this event as a common cause of MSA. The question of a genetic component in MSA remains to be answered.
| Original language | English |
|---|---|
| Pages (from-to) | 340-342 |
| Number of pages | 3 |
| Journal | Parkinsonism and Related Disorders |
| Volume | 13 |
| Issue number | 6 |
| DOIs | |
| State | Published - Aug 2007 |
| Externally published | Yes |
ASJC Scopus Subject Areas
- Neurology
- Geriatrics and Gerontology
- Clinical Neurology
Keywords
- α-Synuclein
- Genomic multiplication
- Multiple system atrophy
- Quantitative PCR
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