Atypical Familial Amyotrophic Lateral Sclerosis Secondary to Superoxide Dismutase 1 Gene Mutation With Coexistent Axonal Polyneuropathy: A Challenging Diagnosis

Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease, is a neurodegenerative disease that involves both the upper and lower motor neurons. Familial ALS, including superoxide dismutase 1 (SOD1) mutation, accounts for 5-10% of all cases of ALS. Typically, the symptoms of ALS ar...

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Detalles Bibliográficos
Autores principales: Makkawi, Seraj, Alqarni, Abdulaziz A, Alghaythee, Himyan, Alharbi, Suzan Y, Fatani, Anmar, Adas, Reem, Abuzinadah, Ahmad R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8817726/
https://www.ncbi.nlm.nih.gov/pubmed/35154965
http://dx.doi.org/10.7759/cureus.20989

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8817726/
https://www.ncbi.nlm.nih.gov/pubmed/35154965
http://dx.doi.org/10.7759/cureus.20989

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