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Brain Volumes in Opsoclonus-Myoclonus Ataxia Syndrome: A Longitudinal Study.
Almudhry, Montaha; Wagner, Matthias W; Longoni, Giulia; Yea, Carmen; Vidarsson, Logi; Ertl-Wagner, Birgit; Yeh, E Ann.
Afiliação
  • Almudhry M; Program in Neurosciences and Mental Health, SickKids Research Institute, The Hospital for Sick Children, Canada.
  • Wagner MW; Division of Neuroradiology, Department of Diagnostic and Interventional Radiology, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Longoni G; Department of Diagnostic and Interventional Neuroradiology, University Hospital Augsburg, Augsburg, Germany.
  • Yea C; Program in Neurosciences and Mental Health, SickKids Research Institute, The Hospital for Sick Children, Canada.
  • Vidarsson L; Division of Neurology, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
  • Ertl-Wagner B; Program in Neurosciences and Mental Health, SickKids Research Institute, The Hospital for Sick Children, Canada.
  • Yeh EA; Division of Neuroradiology, Department of Diagnostic and Interventional Radiology, The Hospital for Sick Children, Toronto, Ontario, Canada.
J Child Neurol ; 39(3-4): 129-134, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38544431
ABSTRACT

INTRODUCTION:

Little is known about the longitudinal trajectory of brain growth in children with opsoclonus-myoclonus ataxia syndrome. We performed a longitudinal evaluation of brain volumes in pediatric opsoclonus-myoclonus ataxia syndrome patients compared with age- and sex-matched healthy children. PATIENTS AND

METHODS:

This longitudinal case-control study included brain magnetic resonance imaging (MRI) scans from consecutive pediatric opsoclonus-myoclonus ataxia syndrome patients (2009-2020) and age- and sex-matched healthy control children. FreeSurfer analysis provided automatic volumetry of the brain. Paired t tests were performed on the curvature of growth trajectories, with Bonferroni correction.

RESULTS:

A total of 14 opsoclonus-myoclonus ataxia syndrome patients (12 female) and 474 healthy control children (406 female) were included. Curvature of the growth trajectories of the cerebral white and gray matter, cerebellar white and gray matter, and brainstem differed significantly between opsoclonus-myoclonus ataxia syndrome patients and healthy control children (cerebral white matter, P = .01; cerebral gray matter, P = .01; cerebellar white matter, P < .001; cerebellar gray matter, P = .049; brainstem, P < .01). DISCUSSION/

CONCLUSION:

We found abnormal brain maturation in the supratentorial brain, brainstem, and cerebellum in children with opsoclonus-myoclonus ataxia syndrome.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Imageamento por Ressonância Magnética / Síndrome de Opsoclonia-Mioclonia Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Imageamento por Ressonância Magnética / Síndrome de Opsoclonia-Mioclonia Idioma: En Ano de publicação: 2024 Tipo de documento: Article