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Movement disorders in adult hydrocephalus

✍ Scribed by Dr. Joachim K. Krauss; Jens P. Regel; Dirk W. Droste; Miro Orszagh; Jan J. Borremans; Werner Vach


Book ID
102947445
Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
721 KB
Volume
12
Category
Article
ISSN
0885-3185

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✦ Synopsis


Abstract

In a prospective series of symptomatic adult hydrocephalus characterized by gait disturbance, cognitive impairment, and/or urinary incontinence, 88 of 118 patients (75%) had additional akinetic, tremulous, hypertonic, or hyperkinetic movement disorders. Their prevalence was highest in patients with idiopathic normal pressure hydrocephalus (NPH) of the elderly (56/65 patients, 86%), and they were less frequent in patients with secondary NPH (10/15, 66%), with nonhydrodynamic atrophic/other hydrocephalus (20/33, 61%), and with obstructive hydrocephalus/aqueductal stenosis (2/5, 40%). Akinetic symptoms were found in 73 of 118 patients (62%), and the most frequent movement disorder was upper extremity bradykinesia (55%). Akinetic, tremulous, hypertonic, and hyperkinetic movement disorders were exclusively secondary to causes not related to hydrocephalus in 24 of 118 patients (20%). The proportion of patients with movement disorders not attributable to only such causes was highest in the idiopathic NPH group (44/65, 68%). Thirteen of 118 patients (11%) presented with a parkinsonian syndrome. There was evidence for coexistent Parkinson's disease in four of these patients. Parkinsonism was found to be secondary to NPH in five patients and was found improved after shunting. Akinetic symptoms in patients with NPH generally responded favorably to CSF diversion, which was evident in 80% of a subset of this group. Various other movement disorders did not show definite improvement. The high prevalence of bradykinesia and other akinetic symptoms in NPH and the beneficial effect of shunting on such symptoms suggest that NPH may cause a more generalized disorder of motor function.


πŸ“œ SIMILAR VOLUMES


The movement disorders of adult opsoclon
✍ Dr. John N. Caviness; Peter A. Forsyth; Donald D. Layton; Thomas J. McPhee πŸ“‚ Article πŸ“… 1995 πŸ› John Wiley and Sons 🌐 English βš– 615 KB

## Abstract We present three cases of the adult opsoclonus‐myoclonus syndrome in patients with systemic carcinoma. In addition to opsoclonus and myoclonus, other clinical components of the syndrome can include ataxia, tremor, gait and stance dysfunction, altered mental status, and head and face dys