A comprehensive review of amyotrophic lateral sclerosis
University of California, Los Angeles · San Juan Bautista School of Medicine
Abstract
Amyotrophic lateral sclerosis (ALS) is a late-onset fatal neurodegenerative disease affecting motor neurons with an incidence of about 1/100,000. Most ALS cases are sporadic, but 5-10% of the cases are familial ALS. Both sporadic and familial ALS (FALS) are associated with degeneration of cortical and spinal motor neurons. The etiology of ALS remains unknown. However, mutations of superoxide dismutase 1 have been known as the most common cause of FALS. In this study, we provide a comprehensive review of ALS. We cover all aspects of the disease including epidemiology, comorbidities, environmental risk factor, molecular mechanism, genetic factors, symptoms, diagnostic, treatment, and even the available…
Citation impact
- FWCI
- 27.02
- Percentile
- 100%
- References
- 354
Authors
10- SZSara ZareiCorresponding
University of California, Los Angeles, San Juan Bautista School of Medicine
- KCKaren Carr
University of California, Los Angeles, San Juan Bautista School of Medicine
- LELuz E. Reiley
University of California, Los Angeles, San Juan Bautista School of Medicine
- KDKelvin Diaz
University of California, Los Angeles, San Juan Bautista School of Medicine
- OGOrleiquis Guerra
University of California, Los Angeles, San Juan Bautista School of Medicine
Topics & keywords
- Amyotrophic lateral sclerosis
- Medicine
- Etiology
- Disease
- Epidemiology
- SOD1
- C9orf72
- Motor neurone disease
- Good health and well-being