Amyotrophic lateral sclerosis classification
Jump to navigation
Jump to search
Amyotrophic lateral sclerosis Microchapters |
Differentiating Amyotrophic lateral sclerosis from other Diseases |
---|
Diagnosis |
Treatment |
Case Studies |
Amyotrophic lateral sclerosis classification On the Web |
American Roentgen Ray Society Images of Amyotrophic lateral sclerosis classification |
Risk calculators and risk factors for Amyotrophic lateral sclerosis classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Charmaine Patel, M.D. [2]Mohamadmostafa Jahansouz M.D.[3]
Overview
ALS is classified into two sub-groups: Familial ALS and Sporadic ALS.
Classification
- Familial ALS accounts for approximately 5%-10% of all ALS cases and is caused due to genetic factors.
- Sporadic ALS accounts for the remaining 90%-95% of ALS with no known cause.
References
- ↑ Hulisz D (2018). "Amyotrophic lateral sclerosis: disease state overview". Am J Manag Care. 24 (15 Suppl): S320–S326. PMID 30207670.