Neuromuscular Junction Disorders

Learning Objectives

1. Understand the pathophysiology of neuromuscular junction disorders, including key mechanisms such as antibody-mediated destruction, genetic mutations, and impaired neurotransmitter release.
2. Identify clinical manifestations and diagnostic criteria of common neuromuscular junction disorders encountered in pediatric critical care, such as myasthenia gravis, Lambert-Eaton myasthenic syndrome, and congenital myasthenic syndromes.
3. Develop proficiency in the management of neuromuscular junction disorders in pediatric critical care settings, including pharmacological interventions, supportive therapies, and considerations for long-term care and rehabilitation.

Pre-Reading Resources

Pediatric Critical Care Outline Specifications

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