Amyotrophic lateral sclerosis

Revision as of 09:59, 24 October 2020 by Rossdonaldson1 (talk | contribs)

Background

  • Progressive muscle atrophy/weakness due to degeneration of upper and lower motor neurons
  • Patients will rarely present to the ED undiagnosed
  • Likely related to mutated superoxide dismutase (SOD1) gene
  • Involvement of the anterior horn cells

Clinical Features

  • Acute respiratory failure
    • Predicted by forced VC <25 mL/kg or 50% decrease from normal
  • Aspiration pneumonia
  • Trauma related to extremity weakness
  • Asymmetric weakness without sensory findings with mixed upper and lower motor nerve findings

Differential Diagnosis

Weakness

Evaluation

Management

Disposition

See Also

External Links

References

Tintinalli's Emergency Medicine: A Comprehensive Study Guide, 7e (2010), Chapter 167. Chronic Neurologic Disorders