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Article

Paroxysmal movement disorders in <i>GLUT1</i> deficiency syndrome

7 Jul 2008

Abstract excerpt

Glucose transporter type I deficiency syndrome ( GLUT1 DS OMIM No. 606777) is an inborn error of glucose transport characterized by seizures, developmental delay, spasticity, acquired microcephaly, and ataxia.1 In addition, in many patients paroxysmal events other than epilepsy have been described,2 but limited information is available regarding their phenomenology and classification. We report on clinical and...

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PMID: 18606970
DOI: 10.1212/01.wnl.0000316804.10020.ba

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