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Illness finder is a diagnostic medicine tool for educational purpose that looks up your patients' health conditions or symptoms and diagnosis and find diseases or illnesses based on chosen gender, age, risk factors, illness, signs, symptoms and prevalence. Illnessfinder is inspired by Evidence based medicine (EMB) and healthcare that aims to apply the best (most reliable) knowledge that is available at decision time. Illnessfinder aims to free up time for the therapeutic dialogue and ensure quality at the evidence based practice, uniting proven medical findings and clinical evidence with systematised data technology.
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| Motor Neuron Disease | Legal notice |
Other terms
Motor Neuron Diseases,Neuron Disease, Motor,Neuron Diseases, Motor,Motor System Disease,Motor System Diseases,Familial Motor Neuron Disease,Motor Neuron Disease, Familial,Lateral Sclerosis,Lateral Scleroses,Scleroses, Lateral,Sclerosis, Lateral,Primary Lateral Sclerosis,Lateral Scleroses, Primary,Lateral Sclerosis, Primary,Primary Lateral Scleroses,Scleroses, Primary Lateral,Sclerosis, Primary Lateral,Motor Neuron Disease, Upper,Upper Motor Neuron Disease,Motor Neuron Disease, Secondary,Secondary Motor Neuron Disease,Anterior Horn Cell Disease,Motor Neuron Disease, Lower,Lower Motor Neuron Disease
Description
Motor Neuron Disease: Diseases characterized by a selective degeneration of the motor neurons of the spinal cord, brainstem, or motor cortex. Clinical subtypes are distinguished by the major site of degeneration. In AMYOTROPHIC LATERAL SCLEROSIS there is involvement of upper, lower, and brainstem motor neurons. In progressive muscular atrophy and related syndromes (see MUSCULAR ATROPHY, SPINAL) the motor neurons in the spinal cord are primarily affected. With progressive bulbar palsy (BULBAR PALSY, PROGRESSIVE), the initial degeneration occurs in the brainstem. In primary lateral sclerosis, the cortical neurons are affected in isolation. (Adams et al., Principles of Neurology, 6th ed, p1089)
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Legal notice
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The version of the data is 2010 MeSH. Last reviewed April 26, 2010. No modification has been made in the content of the file.
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