Characteristic proton magnetic resonance spectroscopy in glucose transporter type 1 deficiency syndrome

Manami Akasaka; Atsushi Kamei; Nami Araya; Kotaro Oyama; Makoto Sasaki

doi:10.1111/ped.13672

Characteristic proton magnetic resonance spectroscopy in glucose transporter type 1 deficiency syndrome

Pediatr Int. 2018 Oct;60(10):978-979. doi: 10.1111/ped.13672. Epub 2018 Oct 15.

Authors

Manami Akasaka¹, Atsushi Kamei¹, Nami Araya¹, Kotaro Oyama¹, Makoto Sasaki²

Affiliations

¹ Department of Pediatrics, School of Medicine, Institute for Biomedical Sciences, Iwate Medical University, Morioka, Iwate, Japan.
² Division of Ultrahigh Field MRI, Institute for Biomedical Sciences, Iwate Medical University, Morioka, Iwate, Japan.

PMID: 30320424
DOI: 10.1111/ped.13672

No abstract available

Keywords: glucose transporter type 1 deficiency syndrome; glutamate-glutamine complex; hypoglycorrhachia; proton magnetic resonance spectroscopy; thalamus.

Publication types

Case Reports

MeSH terms

Carbohydrate Metabolism, Inborn Errors / diagnostic imaging*
Child, Preschool
Glucose Transporter Type 1 / genetics
Humans
Infant
Infant, Newborn
Monosaccharide Transport Proteins / deficiency*
Proton Magnetic Resonance Spectroscopy / methods*

Characteristic proton magnetic resonance spectroscopy in glucose transporter type 1 deficiency syndrome

Authors

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