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Transient regional cerebral hypoperfusion during a paroxysmal hemiplegic event in GLUT1 deficiency syndrome.
Almuqbil, Mohamed; Rivkin, Michael J; Takeoka, Masanori; Yang, Edward; Rodan, Lance H.
Affiliation
  • Almuqbil M; Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA; Division of Pediatric Neurology, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia; King Abdullah International Medical Research Center, King Abdullah Specialist Childre
  • Rivkin MJ; Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA; Department of Psychiatry, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA; Department of Radiology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Takeoka M; Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Yang E; Department of Radiology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Rodan LH; Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA; Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Eur J Paediatr Neurol ; 22(3): 544-547, 2018 May.
Article in En | MEDLINE | ID: mdl-29500071
ABSTRACT
GLUT1 deficiency syndrome (GLUT1DS) is a well described neurometabolic disorder that results from impaired glucose transport into the central nervous system. GLUT1DS classically presents with infantile-onset epilepsy, progressive microcephaly, developmental delay, ataxia, dystonia, and spasticity, but a minority of patients may manifest with paroxysmal non-epileptic phenomena including hemiparesis (Wang et al., 2002). We report for the first time cerebral perfusion changes during an acute episode of hemiparesis in a 9 year old child with GLUT1DS. The patient presented as a code stroke with her second episode of acute-onset left hemiparesis and altered mental status. Emergency MRI of brain demonstrated normal diffusion-weighted imaging, but arterial spin label perfusion weighted imaging (ASL-PWI) showed regional hypoperfusion of the right cerebral hemisphere and magnetic resonance angiography (MRA) revealed distally restricted flow related enhancement in the right MCA. The patient's deficits resolved entirely within several hours from onset. Repeat MRI one month later was normal. Our report suggests that GLUT1DS-related hemiplegic events are associated with transient lateralized cerebrovascular hypoperfusion similar to that described in hemiplegic migraine and other pediatric stroke mimics. The underlying pathophysiology for this phenomenon in GLUT1DS is not known, but may relate to cortical energy failure or abnormal cerebral microvasculature.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Monosaccharide Transport Proteins / Carbohydrate Metabolism, Inborn Errors / Brain Ischemia / Hemiplegia Limits: Child / Female / Humans Language: En Journal: Eur J Paediatr Neurol Journal subject: NEUROLOGIA / PEDIATRIA Year: 2018 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Monosaccharide Transport Proteins / Carbohydrate Metabolism, Inborn Errors / Brain Ischemia / Hemiplegia Limits: Child / Female / Humans Language: En Journal: Eur J Paediatr Neurol Journal subject: NEUROLOGIA / PEDIATRIA Year: 2018 Document type: Article