Infantile Neuroglycopenia
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 neu...
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| Format: | Book |
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Pediatric Neurology Briefs Publishers,
2007-05-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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| Summary: | 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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| Item Description: | 1043-3155 2166-6482 10.15844/pedneurbriefs-21-5-3 |