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[Bobble-head doll syndrome].

Abstract
A new case of Bobble-head doll syndrome with aqueductal stenosis is presented in a 14 year-old boy. Ventriculocisternostomy performed 8 years after the onset of the abnormal movement resulted in moderate reduction of the head bobbling. Twenty-two cases were found in a review of the literature. In all cases there was a chronic slowly progressive hydrocephalus with usually a cyst of the third ventricle; aqueductal stenosis was less frequent. When recorded, psychomotor development was impaired. Treatment is neurosurgical. Pathogenesis remains unknown.
AuthorsA Roubergue, P Beauvais, J M Richardet
JournalArchives francaises de pediatrie (Arch Fr Pediatr) Vol. 42 Issue 5 Pg. 377-8 (May 1985) ISSN: 0003-9764 [Print] France
Vernacular TitleSyndrome de la poupée à tête ballotante. "Bobble-head doll syndrome".
PMID4074089 (Publication Type: Case Reports, English Abstract, Journal Article)
Topics
  • Adolescent
  • Brain Diseases (complications)
  • Cerebral Aqueduct
  • Head
  • Humans
  • Hydrocephalus (etiology)
  • Male
  • Movement Disorders (etiology)

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