A case of camptocormia (bent spine) secondary to early motor neuron disease

Abstract. Camptocormia is a gait disorder, characterized by hyperflexion of thoracolumbar spine which increases on walking, and disappears in the supine position. A 48 year-old man developed progressive gait deterioration for one year and slight weakness and tremor of both hands for five months. It eventually became apparent that the patient had motor neuron disease, as well as symptoms of extrapyramidal disorder

A Case of Camptocormia (Bent Spine) Secondary to Early Motor Neuron Disease

Camptocormia is a gait disorder, characterized by hyperflexion of thoracolumbar spine which increases on walking, and disappears in the supine position

Chorea as the presentating feature of neurosyphilis

Syphilis is still a significant public health problem in developing countries. Although chorea is a very rare manifestation of neurosyphilis, it might be on occasions the initial symptom. This report presents a patients with neurosyphilis who had chorea as the initial presenting symptom

The Relationship Between Carotid Intima-media Thickness and Homosystein in Ischemic Stroke

Objective: The vast majority of ischemic strokes occur due to atherosclerosis. Although the precise mechanism is unknown, high homocysteine (HM) levels are considered to play a role in the development of atherosclerosis. In this study, the relationship between high HM and carotid intima-media thickness (CIMT), as an early predictor of atherosclerosis, is evaluated in patients with ischemic stroke

Camptocormia in a patient with Parkinson disease and a myopathy with nemaline rods

Camptocormia, also referred to as bent spine, is a gait disorder characterized by hyperflexion of the thoracolumbar spine that develops in recumbent position while walking and that disappears in supine position. Myopathy is one of the frequent causes of camptocormia. A 77-yr-old male patient who was followed up with the diagnosis of rheumatoid arthritis for 2 yrs was admitted with progressive gait deterioration. Hyperflexion of trunk, disappearing in supine position, was detected and diagnosed as camptocormia. He also exhibited the signs of parkinsonism. A paraspinal muscle biopsy showed myopathy with rods in many muscle fibers. Camptocormia in this patient may be attributable to the myopathic weakness of thoracolumbar paraspinal muscles. The normal biceps brachii muscle biopsy refers to the isolated affection of paraspinal muscles in this patient. A camptocormia (bent spine) case of myopathy with nemaline rods associated with Parkinson disease is presented