Pediatric Neurology Briefs
Published 2007 | Version v1.0.0
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Infantile Neuroglycopenia

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Abstract

Participant 1, a 23-year-old woman with congenital hypoglycemia (hyperinsulinism); participant 2, a 16-year-old boy with genetic mutation of the cerebral glucose transporter type 1 (GLUT1 deficient); and participant 3, the 23-year-old healthy twin sister of participant 1 as a control, received a neurologic examination, PET scan, and neuropsychological evaluation, in a study at Neurological Institute, New York, NY.

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PNB-21-35

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Created
2007
When the item was originally created.