Infantile Neuroglycopenia
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.
DOI: https://doi.org/10.15844/pedneurbriefs-21-5-3 | Journal eISSN: 2166-6482
Language: English
Page range: 35 - 35
Published on: May 1, 2007
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 2007 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.