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Head drop and camptocormia

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TLDR
The evaluation of these disorders can indeed be challenging and often no definite diagnosis is made, as illustrated by four cases of head ptosis and camptocormia seen by us at the Johns Hopkins Hospital.
Abstract
The spectrum of bent spine disorders Head ptosis (drop) results from weakness of the neck extensor, or increased tone of the flexor muscles. It is characterised by marked anterior curvature or angulation of the cervical spine and is associated with various neuromuscular (table 1) and extrapyramidal disorders.12–15 Camptocormia or the bent spine syndrome was first described in hysterical soldiers in 1915 by the French neurologist Souques.16 Typically there is marked anterior curvature of the thoracolumbar spine. In some patients the spine is angulated forward, the arms propped against the thigh for support. More cases, all among soldiers, were reported during the first and second world wars. These patients responded well to psychotherapy. Recently camptocormia arising as a result of weakness or abnormality in the tone of the paraspinal muscles has been described (table 2). In contrast with other skeletal disorders of the spine such as kyphosis, the deformity in head ptosis and camptocormia is not fixed and is corrected by passive extension or lying in the supine position. It is not possible to straighten the neck or back voluntarily. The evaluation of these disorders can indeed be challenging and often no definite diagnosis is made, as illustrated by four cases of head ptosis and camptocormia seen by us at the Johns Hopkins Hospital. View this table: Table 1 Neuromuscular causes for head ptosis View this table: Table 2 Causes of camptocormia An 80 year old man developed head ptosis insidiously over a period of few weeks. A week before this he had an upper respiratory tract infection and also experienced transient sharp pain over the left and then the right shoulder. He had no diplopia, dysarthria, dysphagia, limb weakness, or fatiguability. Examination showed severe neck extensor weakness, Medical Research Council (MRC) grade 2. Muscle strength was normal in all other cranial, proximal, and distal limb muscles. Serum …

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Motor fluctuations and dyskinesias in Parkinson's disease: clinical manifestations.

TL;DR: The most common type of dyskinesia, called “peak‐dose dyskinese”, usually consists of stereotypical choreic or ballistic movements involving the head, trunk, and limbs, and occasionally, the respiratory muscles, whereas tremor and punding are less‐common complications.
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Camptocormia: Pathogenesis, classification, and response to therapy

TL;DR: Etiologic classification of camptocormia is proposed and it is concluded that this heterogeneous disorder has multiple etiologies and variable response to systemic and local therapies.
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A weak balance: the contribution of muscle weakness to postural instability and falls.

TL;DR: It is concluded that muscle weakness is an important risk factor for falls that is potentially amenable to therapeutic intervention, and that future studies should further clarify the role of muscle weakness in balance control and the pathophysiology of falls.
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Joint and skeletal deformities in Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy

TL;DR: 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.
Journal ArticleDOI

Parkinson’s disease with camptocormia

TL;DR: Patients with camptocormia were characterised by prominent levodopa-unresponsive axial symptoms (ie, axial rigidity, gait disorder and postural instability), along with a tendency for greater error in the antisaccade paradigm, and it is suggested that the salient features of parkinsonism observed in patients with camps are likely to represent a specific form of Parkinson’s disease.
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