## Abstract The clinical features of multiple system atrophy (MSA) include four domains: autonomic failure/urinary dysfunction, Parkinsonism, cerebellar ataxia, and corticospinal tract dysfunction. Although the diagnosis of definite MSA requires pathological confirmation, magnetic resonance imaging
Pyramidal tract imaging in multiple-system atrophy
โ Scribed by Nicole Limberg; Susanne Jeavons; Thomas Robertson; Richard Boyle
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 97 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0885-3185
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
A new radiological finding of T2 FLAIR hyperintensities in the pyramidal tracts is described in a patient clinically thought to have idiopathic Parkinson's disease but histologically proven to have multipleโsystem atrophy. ยฉ 2005 Movement Disorder Society
๐ SIMILAR VOLUMES
## Abstract We here report survival in patients with multiple system atrophy (MSA) in a large, prospectively studied group of patients with MSA. Eightyโfive of 100 patients were known to have died. Three patients were rediagnosed as having PD. Twentyโfour patients came to autopsy, which showed MSA
This review provides an update on therapeutic principles and their implications for practical management in multiple system atrophy (MSA), a sporadic neurodegenerative disorder characterized clinically by various combinations of dysautonomia, Parkinsonism, or cerebellar ataxia, often associated with
## Abstract Two patients are described with clinical and neuroimaging features consistent with a diagnosis of multiple system atrophy (MSA). The patients are unusual in that facial myokymia became apparent clinically at some stage in their illness. In each patient, the nature and severity of the in
## Abstract Multiple system atrophy can be classified into two main types, a Parkinsonian (MSAโP) and a cerebellar (MSAโC) variant based on clinical presentation. We obtained diffusionโweighted magnetic resonance imaging (DWI) in 9 MSAโP and 12 MSAโC patients and 11 controls, and correlated DWI cha
Patients with multiple system atrophy (MSA) have a mean survival of 8 to 10 years. Nocturnal stridor has been considered a poor prognostic feature. We analyzed demographic, clinical, and polysomnographic data and obtained follow-up information from 42 patients with MSA (30 with follow-up data) seen