๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Abnormal temporal discrimination threshold in patients with multiple system atrophy

โœ 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

No coin nor oath required. For personal study only.

โœฆ 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 wellโ€controlled 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 ageโ€matched 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


๐Ÿ“œ SIMILAR VOLUMES


Camptocormia in a patient with multiple
โœ Frank Skidmore; Irene Mikolenko; Howard Weiss; William Weiner ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 77 KB ๐Ÿ‘ 1 views

## Abstract The term โ€œcamptocormiaโ€ describes a severe forwardโ€flexed posture. Although initially used to describe a conversion disorder, early authors also recognized organic camptocormia occurring in old age, or โ€œcamptocormie senile,โ€ as well as traumatic and arthritic camptocormia. More recently

Myoclonic tremor in patients with parkin
โœ Yasuyuki Okuma; Yoshikuni Mizuno ๐Ÿ“‚ Article ๐Ÿ“… 2001 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 17 KB

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

Depressive symptoms and life satisfactio
โœ Lisa M. Benrud-Larson; Paola Sandroni; Anette Schrag; Phillip A. Low ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 76 KB ๐Ÿ‘ 1 views

## 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

Pathological laughter and crying in pati
โœ Josef Parvizi; Jeffrey Joseph; Daniel Z. Press; Jeremy D. Schmahmann ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 146 KB

## Abstract In the cerebellar type of multiple system atrophy (MSAโ€C), 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