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Updated: Jul 11, 2026

Utility of Dissociated Intrinsic Hand Muscle Atrophy in the Diagnosis of Amyotrophic Lateral Sclerosis
Published on: March 4, 2014
[Simultaneous presentation of amyotrophic lateral sclerosis and multiple sclerosis]
B Machner1, S Gottschalk, H Kimmig
1Klinik für Neurologie, Universitätsklinikum Schleswig-Holstein, Campus Lübeck, Ratzeburger Allee 160, Lübeck, Germany. Bjoern.Machner@neuro.uni-luebeck.de
This case report details a rare instance of concurrent amyotrophic lateral sclerosis (ALS) and multiple sclerosis (MS). It highlights the diagnostic challenges and emphasizes considering motor neuron diseases in MS patients with significant peripheral denervation.
Area of Science:
- Neurology
- Neuroimmunology
Background:
- Amyotrophic lateral sclerosis (ALS) and multiple sclerosis (MS) are distinct neurological disorders.
- The co-occurrence of ALS and MS is exceptionally rare in clinical practice.
Observation:
- A 55-year-old female presented with progressive gait and speech disorders.
- Initial findings met diagnostic criteria for MS, including MRI and CSF analysis.
- Subsequent development of generalized fasciculations, muscle atrophy, and bulbar signs met ALS criteria.
Findings:
- Nerve conduction studies revealed widespread acute and chronic denervation without conduction block.
- The patient was diagnosed with the unusual concurrent combination of ALS and MS.
- Myelitic lesions in MS can cause peripheral denervation, but the generalized nature suggested co-existing ALS.
Implications:
- This case underscores the importance of considering motor neuron diseases in MS patients exhibiting pronounced peripheral denervation.
- Early recognition of co-existing ALS and MS is crucial for appropriate patient management.
- Highlights the complex differential diagnosis in neurodegenerative and autoimmune conditions.
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