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Journal ArticleDOI

Joint and skeletal deformities in Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy

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TLDR
Clinical features of joint and skeletal deformities in Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy are characterized to cause marked functional disability independent of other motor symptoms.
Abstract
The objective of this study is to characterize clinical features of joint and skeletal deformities in Parkinson's disease (PD), multiple system atrophy (MSA), and progressive supranuclear palsy (PSP). Clinical information including age, gender, presence of deformity, initial symptom side, neuropsychological and motor features, family history, and treatment with levodopa/dopamine agonists was collected on consecutive patients with PD, MSA, and PSP evaluated at the Movement Disorders Clinic at Baylor College of Medicine. In this series of 202 patients, 36.1% had deformities of the limbs, neck, or trunk, including 33.5% of PD, 68.4% of MSA, and 26.3% of PSP patients. "Striatal" hand and foot deformities were present in 13.4%, involuntary trunk flexion in 12.9%, anterocollis in 9.4%, and scoliosis in 8.4% of all patients. Patients with these joint and skeletal deformities had higher mean Unified Parkinson's Disease Rating Scale scores (57.4 vs. 46.6; P < 0.01) and were more often treated with levodopa (69.9% vs. 50.4%; P < 0.01) than patients without deformity, independent of disease duration. Patients with striatal deformity were younger than patients without deformity (mean 60.4 vs. 68.6 years; P < 0.01), and they tended to have an earlier age of onset of initial parkinsonian symptoms (mean 54.7 vs. 62.5 years; P < 0.01). Furthermore, the side of striatal deformity correlated with the side of initial parkinsonian symptoms in all patients (100%) with striatal hand and in 83.3% of patients with striatal foot. Joint and skeletal deformities are common and frequently under-recognized features of PD, MSA, and PSP that often cause marked functional disability independent of other motor symptoms.

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TL;DR: A framework for understanding balance dysfunction in PD is described to help clinicians recognize patients who are at risk for falling and impaired mobility.
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Pains in Parkinson disease--many syndromes under one umbrella.

TL;DR: A four-tier taxonomy to improve classification of pain in Parkinson disease is proposed, which assigns nociceptive, neuropathic and miscellaneous pains to distinct categories, as well as further characterization into subcategories.
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Pain in Parkinson's disease.

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References
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Journal ArticleDOI

Dystonia in progressive supranuclear palsy.

TL;DR: Dystonia is a common manifestation of PSP and may indicate the presence of concurrent disease, and dopaminergic medication should be cautiously reduced or discontinued to rule out the possibility of treatment induced symptoms.
Journal ArticleDOI

Cholinergic-dopaminergic imbalance in Pisa syndrome

TL;DR: Two patients, one with Alzheimer's disease treated with risperidone and another with Parkinson's disease who presented this kind of dystonia after donepezil initiation are reported.
Journal ArticleDOI

Striatal deformities of the hand and foot in Parkinson's disease.

TL;DR: The background and clinical features of striatal deformities of the hand and foot are reviewed to highlight these commonly unrecognised and poorly understood parkinsonian signs.
Journal ArticleDOI

Treatment of dystonic clenched fist with botulinum toxin.

TL;DR: Four patients with Parkinson's disease and one patient with Dystonia‐Complex Regional Pain Syndrome obtained functional benefit with BTXA, and palmar infection, when present, was eradicated.
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