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: | , , , , |
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| Format: | Book |
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Wiley,
2022-03-01T00:00:00Z.
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