International Journal For Multidisciplinary Research

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A Widely Indexed Open Access Peer Reviewed Multidisciplinary Bi-monthly Scholarly International Journal

Call for Paper Volume 6 Issue 3 May-June 2024 Submit your research before last 3 days of June to publish your research paper in the issue of May-June.

Bobble Head Doll Syndrome Revealing a Suprasellar Arachnoid Cyst : Case Report

Author(s) BAHBOUH Siham, BOUAITA Kamel
Country Algérie
Abstract Introduction
Bobble head doll syndrome (BHDS) is a rare neurological syndrome that appears in childhood. It is characterized by abnormal movements of the head, most commonly in an up-and-down motion ("yes yes") and rarely in the horizontal plane ("no no"). We report a case of BHDS revealing a large suprasellar arachnoid cyst.
Observation
A 6-year-old child was brought by his parents to a neurology consultation for abnormal head movements, which most frequently occurred in an upward and downward direction, but disappeared during sleep. These abnormal movements had been progressively worsening over the course of approximately one year. Clinical examination revealed a decrease in visual acuity in both eyes, with papillary hyperemia on fundoscopy and discreet ataxia in walking. Magnetic resonance imaging (MRI) revealed a compressive suprasellar arachnoid cyst with passive biventricular hydrocephalus. Surgical treatment with neuro-endoscopy led to a remarkable regression of abnormal head movements and ataxia in the immediate postoperative period, with complete disappearance in the long term.
Conclusion
Bobble head doll syndrome is a potentially "curable" entity, and diagnosis is provided by cerebral MRI.
Keywords Bobble head doll syndrome, suprasellar arachnoid cyst, neuro-endoscopy
Field Médical / Pharmacie
Published In Volume 6, Issue 2, March-April 2024
Published On 2024-04-27
Cite This Bobble Head Doll Syndrome Revealing a Suprasellar Arachnoid Cyst : Case Report - BAHBOUH Siham, BOUAITA Kamel - IJFMR Volume 6, Issue 2, March-April 2024. DOI 10.36948/ijfmr.2024.v06i02.18566
DOI https://doi.org/10.36948/ijfmr.2024.v06i02.18566
Short DOI https://doi.org/gtsg4v

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