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The Ketogenic Diet in Children with Glut1 Deficiency Syndrome and Epilepsy

✍ Scribed by Markus Rauchenzauner; Jörg Klepper; Bärbel Leiendecker; Gerhard Luef; Kevin Rostasy; Christoph Ebenbichler


Book ID
113744729
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
90 KB
Volume
153
Category
Article
ISSN
1097-6833

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## Abstract Glucose transport protein deficiency due to mutation in the __GLUT1__ gene is characterized by infantile onset and chronic seizure disorder, microcephaly, global developmental delays, and hypoglycorrhachia. We describe a 10‐year‐old normocephalic male with prominent ataxia, dystonia, ch