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Head bobbing in a patient with a cyst of the third ventricle

Child'S Brain
|January 1, 1978
PubMed

Insights

Bobble head doll syndrome, a rare childhood movement disorder, is often linked to third ventricle cysts. Surgical removal of these cysts provides only slight symptom improvement, suggesting complex underlying mechanisms.

Area of Science:

  • Neurology
  • Pediatrics
  • Neuroscience

Background:

  • Bobble head doll syndrome is a rare movement disorder characterized by rhythmic head bobbing, typically emerging in early childhood.
  • The condition is often associated with lesions in the anterior third ventricle region.

Observation:

  • A case report details a 7-year-old boy with bobble head doll syndrome and a third ventricle cyst.
  • Partial cyst removal via transcortical exploration resulted in minimal reduction of the head bobbing tic.
  • A literature review identified 17 cases, with an average age of 7 years at diagnosis.

Findings:

  • In 13 of the 17 reviewed cases, a slow-growing cyst or mass in or near the anterior third ventricle was identified as the cause.
  • Acute lesions were not observed as a cause.
  • Aqueductal stenosis was suspected in 3 cases, and the cause remained unknown in 1 case.

Implications:

  • The findings highlight the strong association between third ventricle cysts and bobble head doll syndrome in children.
  • The limited efficacy of surgical intervention suggests that the pathophysiology of this syndrome may involve more than just physical obstruction.
  • Further research is needed to elucidate the precise mechanisms and explore more effective treatment strategies for this condition.

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