| Literature DB >> 21382692 |
Abstract
GLUT1 deficiency syndrome (GLUT1DS) is caused by impaired glucose transport into brain and is effectively treated by means of a ketogenic diet. In clinical practice the diagnosis of GLUT1DS often is challenging due to the increasing complexity of symptoms, diagnostic cut-offs for hypoglycorrhachia and genetic heterogeneity. In terms of treatment alternative ketogenic diets and their long-term side effects as well as novel compounds such as alpha-lipoic acid and triheptanoin have raised a variety of issues. The current diagnostic and therapeutic approach to GLUT1DS is discussed in this review in view of these recent developments.Entities:
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Year: 2011 PMID: 21382692 DOI: 10.1016/j.eplepsyres.2011.02.007
Source DB: PubMed Journal: Epilepsy Res ISSN: 0920-1211 Impact factor: 3.045