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Updated: Aug 15, 2025

A Protocol for Comprehensive Assessment of Bulbar Dysfunction in Amyotrophic Lateral Sclerosis ALS
Published on: February 21, 2011
Coexisting amyotrophic lateral sclerosis and chorea: A case report and literature review
Anni Zhang1, Hongbei Xu, Jing Huang
1Department of Neurology, Affiliated Hospital of Guizhou Medical University, Guizhou, China.
Background:
Amyotrophic lateral sclerosis (ALS) coexisting with chorea is very rare.
Case Report:
We present the case of a 48-year-old man with ALS and chorea; the diagnostic certainty was high based on clinical examination results. Combining the data from literature, we analyzed the characteristics of patients with ALS and chorea. We found that ALS coexisting with chorea is very rare, but is often hereditary with a genetic mutation. Most patients with ALS and chorea are caused by abnormal amplification of a CAG sequence in the HTT gene, and these patients have a mild course of disease. The FUS, VCP, and SETX genes also have low mutation frequencies in patients with ALS and chorea.
Conclusion:
The abnormal amplification of a CAG sequence in the HTT gene in ALS with chorea has an obvious familial genetic tendency, and most patients have a mild disease course.
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