## Abstract The term โcamptocormiaโ describes a severe forwardโflexed posture. Although initially used to describe a conversion disorder, early authors also recognized organic camptocormia occurring in old age, or โcamptocormie senile,โ as well as traumatic and arthritic camptocormia. More recently
Abnormal temporal discrimination threshold in patients with multiple system atrophy
โ Scribed by Chul H. Lyoo; Seung Yeob Lee; Tae Jin Song; Myung Sik Lee
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 103 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0885-3185
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โฆ Synopsis
Abstract
The temporal discrimination threshold (TDT), the shortest time interval that allows two temporally separated successive stimuli to be perceived as two different stimuli, is a constituent of kinesthetic sensation. Intact kinesthesia is a necessity for wellโcontrolled voluntary movements. In patients with Parkinson's disease and dystonia, abnormally increased TDT has been reported and it may contribute to the pathophysiology of motor deficits. We explored the integrity and clinical significance of TDT in patients with multiple system atrophy (MSA). A total of 30 de novo patients with MSA and 11 ageโmatched normal controls were included. The TDT values were measured in the feet with four different paradigms (ascending and descending interstimuli intervals; same and different point stimulation). The Unified Parkinson's Disease Rating Scale (UPDRS) Motor and the International Cooperative Ataxia Rating Scale (ICARS) scores were measured for parkinsonian and cerebellar deficits, respectively. Means of the TDT values of the patients with MSA were higher than those of the controls. The TDT values correlated with UPDRS Motor scores independent of ICARS scores. Among the parkinsonian motor deficits, only the UPDRS Motor subscores representing bradykinesia correlated with the TDT values. In patients with MSA, abnormal somatic sensory processing seems to be associated with damage to the nigrostriatal dopaminergic and/or striatal neurons. ยฉ 2007 Movement Disorder Society
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We read with great interest the paper by Salazar and colleagues, analyzing postural and action myoclonus in patients with parkinsonian-type multiple system atrophy (pMSA). 1 We agree with their observation that abnormal involuntary movements (AIMs) involving fingers and hands are frequently seen in
## Abstract Multiple system atrophy (MSA) is a progressive neurodegenerative disorder characterized by extrapyramidal signs, prominent autonomic failure, and a poor prognosis. In the absence of restorative treatment, management is aimed at improving quality of life. Little is known about modifiable
## Abstract In the cerebellar type of multiple system atrophy (MSAโC), the burden of pathological changes involves the cerebellum and its associated brainstem structures in the basis pontis and the inferior olivary nucleus, and as a result, the clinical phenotype is dominated early on by the cerebe