GLUT-1 deficiency without epilepsy--an exceptional case.

Article Details

Citation

Overweg-Plandsoen WC, Groener JE, Wang D, Onkenhout W, Brouwer OF, Bakker HD, De Vivo DC

GLUT-1 deficiency without epilepsy--an exceptional case.

J Inherit Metab Dis. 2003;26(6):559-63.

PubMed ID
14605501 [ View in PubMed
]
Abstract

The GLUT-1 deficiency is a metabolic disorder caused by a defect in glucose transport across the blood-brain barrier as a result of a defect in the glucose-transport protein. Patients present with epileptic seizures, delayed development, ataxia and hypotonia, and in many cases acquired microcephaly. In most patients, treatment with a ketogenic diet proved to be successful in controlling the epilepsy. We report a 9-year-old boy with retardation and ataxia, but without epilepsy, caused by GLUT-1 deficiency, proven biochemically and by DNA analysis. Treatment with a medium-chain triglyceride ketogenic diet had a beneficial effect.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Solute carrier family 2, facilitated glucose transporter member 1P11166Details