Pediatric Movement Disorders

A movement disorder may be a condition that arises within the brain that causes a baby to move insufficient or too little. Movement disorders will arise from medication, infection, brain injury, autoimmune disease or they'll be inheritable.

This session explains that there is increasing evidence that these disorders are autoimmune and are mediated by antibodies against cell surface or synaptic proteins and cause dysfunction within the central nervous system. Hemiplegia of childhood and rapid onset dystonia-parkinsonism are two separate movement disorders with different dominant mutations in the same gene and Myoclonus shows sudden, brief, shock like movements that may be repetitive or rhythmic.

  • Myoclonus
  • Hemiplegia of childhood and rapid onset dystonia-parkinsonism
  • Movement disorders associated with antibodies against cell surface or synaptic proteins

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