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Amyotrophic Lateral Sclerosis

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amyotrophic lateral sclerosis

[¦a′mī·ə¦träf·ik ′la·trəl sklə′rō·səs]
(medicine)
A progressive neurological disorder characterized by loss of connection and death of motor neurons in the cortex and spinal cord.
McGraw-Hill Dictionary of Scientific & Technical Terms, 6E, Copyright © 2003 by The McGraw-Hill Companies, Inc.
The following article is from The Great Soviet Encyclopedia (1979). It might be outdated or ideologically biased.

Amyotrophic Lateral Sclerosis

 

an organic disease of the central nervous system, with predominant affection of the spinal cord and medulla oblongata. First described in 1865 by the French neuropathologist J. Charcot.

About 3 percent of all organic lesions of the central nervous system are due to amyotrophic lateral sclerosis, which is observed mainly in the 30- to 50-year age group. The causes of the disease are unknown. The majority of scientists regard the condition as degenerative, but a theory of viral causation is being developed. The onset of amyotrophic lateral sclerosis is accompanied by gradually intensifying weakness of arms and legs. Swallowing and speech become impaired in proportion to the progress of the disease. As a result of weakness of the muscles of the tongue, soft palate, and vocal cords, choking occurs during eating, food enters the nose, and speech becomes nasalized and sometimes completely impossible. Tendon reflexes of the arms and legs are intensified, and pathological reflexes appear. Sensitivity disorder is occasionally present. Amyotrophic lateral sclerosis is chronic.

Treatment Medicinal preparations which benefit the central nervous system and the metabolism in damaged tissues (lipotserebrin, dibazol, proserine, vitamins B12, B1 and E), and physiotherapy. Constant and attentive care of the patient is necessary.

REFERENCE

Khondkarian, O. A. “Bokovoi amiotroficheskii skleroz.” In Mnogotomnoe rukovodstvo po nevrologii, vol. 3, book 1. Edited by S. N. Davidenkov. Moscow, 1962. (A bibliography is included.)

V. S. ROTENBERG

The Great Soviet Encyclopedia, 3rd Edition (1970-1979). © 2010 The Gale Group, Inc. All rights reserved.
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References in periodicals archive
The value of magnetic resonance imaging as a biomarker for amyotrophic lateral sclerosis: A systematic review.
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder characterized by upper motor neuron, corticospinal tract, and lower motor neuron involvement.
Hardiman et al., "A revision of the El Escorial criteria-2015," Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, vol.
Preliminary results of national amyotrophic lateral sclerosis (ALS) registry risk factor survey data.
El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases and the El Escorial "Clinical limits of amyotrophic lateral sclerosis" workshop contributors.
Swash, "The expanding syndrome of amyotrophic lateral sclerosis: a clinical and molecular odyssey," Journal of Neurology, Neurosurgery, and Psychiatry, vol.
Differential diagnoses in amyotrophic lateral sclerosis. Philadelphia, PA: FA.
Amyotrophic lateral sclerosis has a poor prognosis, with the incidence rate of 0.4-2.5 cases per 100 000 people per year, and a mortality rate of 0.8-2.1 cases per 100 000 people per year.
INTRODUCTION: Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that affects the upper and the lower motor neurons in the cerebral cortex, brainstem, and spinal cord.
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