Abnormal gait and hypoglycorrhachia in a toddler with seizures

ABSTRACT Introduction Glucose transporter type 1 (Glut1) deficiency syndrome is a treatable neurometabolic disorder characterized by seizures, developmental delay, and hypoglycorrhachia. Due to the rareness and non‐specific clinical manifestations, it is usually mis‐ or underdiagnosed. Case presenta...

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Main Authors: Maria Angeli (Author), Eleni Vergadi (Author), Georgios Niotakis (Author), Maria Raissaki (Author), Emmanouil Galanakis (Author)
Format: Book
Published: Wiley, 2022-03-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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