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Updated: Feb 14, 2026
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Eye-Tracking Control to Assess Cognitive Functions in Patients with Amyotrophic Lateral Sclerosis
Published on: October 13, 2016
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[Laryngospasm in amyotrophic lateral sclerosis : A case report]
Andrea Spielberger1, Stefan Lorenzl2
1Abteilung für Neurologie, Palliativeinheit, LKH Murtal, Standort Knittelfeld, Gaalerstraße 10, 8720, Knittelfeld, Österreich. andrea.spielberger@gmx.net.
Wiener Medizinische Wochenschrift (1946)
|February 17, 2018
Summary
Laryngospasm, a rare symptom in amyotrophic lateral sclerosis (ALS), presents a life-threatening condition despite its self-limiting nature. This report explores its causes and therapeutic strategies for ALS patients.
Area of Science:
- Neurology
- Pulmonology
Background:
- Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease affecting nerve cells in the brain and spinal cord.
- Laryngospasm is a sudden, abnormal contraction of the vocal cords, leading to breathing difficulties.
Observation:
- Laryngospasm is an infrequently documented symptom in the context of amyotrophic lateral sclerosis.
- While typically self-limiting, laryngospasm can pose a significant, immediate threat to life in ALS patients.
Findings:
- The underlying mechanisms contributing to laryngospasm in ALS require further investigation.
- Potential therapeutic interventions for managing laryngospasm in ALS patients are discussed.
Implications:
- Recognizing laryngospasm as a potential ALS complication is crucial for timely intervention.
- Further research into the pathophysiology and treatment of laryngospasm in ALS is warranted to improve patient outcomes.
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