Glut-1 Deficiency Syndrome and Familial Epilepsy

Authors

J Gordon Millichap Northwestern University Feinberg School of Medicine

DOI:

https://doi.org/10.15844/pedneurbriefs-15-10-2

Keywords:

Deficiency Syndrome, Antiepileptic Drugs, Mild Ataxia-Dystonia

Abstract

A family with autosomal dominant Glut-1 deficiency syndrome (DS) affecting 5 members over 3 generations is reported from the University of Goettingen, Germany; and Columbia University, New York.

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Published

2001-10-01

Issue

Vol 15, No 10 | Oct 2001

Section

Metabolic Disorders

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