2021, Number 02
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Revista Médica Sinergia 2021; 6 (02)
Initial clinical management of amioatrophic lateral sclerosis
Charpentier MRJ, Loaiza QKV
Language: Spanish
References: 18
Page: 1-12
PDF size: 187.26 Kb.
ABSTRACT
Amyotrophic lateral sclerosis is a progressive disease characterized by degeneration of motor neurons
in the brain and spinal cord. There are two fundamental forms of this disease: the sporadic form and the
familial form. There is still no clarity about its etiology. Clinical manifestations include signs of damage to
the upper and lower motor neurons, both in the extremities and in the bulbar musculature. The diagnosis
continues to be fundamentally clinical, supported by neurophysiological studies. There is no curative
treatment. Riluzole is the first-line drug treatment that has been shown to delay the normal course of the
disease. Edaravone is approved by the FDA for use in this disease in conjunction with riluzole.
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