## Abstract Camptocormia (CC) or pronounced forward flexion of the trunk is a common symptom of Parkinson's disease. We describe 2 patients with probable, respectively possible multipleโsystem atrophy and CC. Magnetic resonance imaging of the erector trunci showed focal patchy hyperintensities with
Camptocormia in a patient with multiple system atrophy
โ Scribed by Frank Skidmore; Irene Mikolenko; Howard Weiss; William Weiner
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 77 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0885-3185
No coin nor oath required. For personal study only.
โฆ Synopsis
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, camptocormia has been described in patients with Parkinson's disease and in an individual with parkinsonism. We describe a case of progressive camptocormia as part of the initial presentation of a patient with multiple system atrophy. ยฉ 2005 Movement Disorder Society
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To note, none of the other occasionally tested protocols (mono polar STIM or 50/70/130 Hz or even 4-4.5 V) provided better results. b Better turning in bed, nighttime, with respect to PPTg-OFF condition. c Improved rigidity (left arms) and slightly improved finger tapping, bilaterally, with respects
## Abstract The cerebellar variant of multiple system atrophy (MSAโC) has overlapping clinical features with the hereditary spinocerebellar ataxias (SCAs), but can usually be distinguished on a clinical basis. We describe a patient who developed a sporadic, lateโonset, rapidly progressive neurodege
## 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.
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