An update on recent amyotrophic lateral sclerosis developments Prognostic categories for amyotrophic lateral sclerosis
Received Date: Mar 02, 2023 / Published Date: Mar 30, 2023
Abstract
The name of the motor neuron disease with the highest prevalence is amyotrophic lateral sclerosis (ALS). It usually has adult-onset degeneration of the upper and lower motor neurons and results in mortality a few years after beginning. Several of the known mutant genes present in familial cases of the disease have also been detected in sporadic forms of the disease. A percentage of ALS patients have an inherited form of the disease. The many ALS-linked gene products, which affect the disease's course and diminish voluntary motor capacity, are not completely understood. This review explores the important developments in our understanding of the disease's underlying underpinnings, which could someday result in new therapeutic choices.
Citation: Canario A (2023) An update on recent amyotrophic lateral sclerosis developments Prognostic categories for amyotrophic lateral sclerosis. J Clin Exp Neuroimmunol, 8: 174.
Copyright: © 2023 Canario A. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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