Glut-1 Deficiency Syndrome and Familial Epilepsy

J Gordon Millichap

doi:10.15844/pedneurbriefs-15-10-2

Glut-1 Deficiency Syndrome and Familial Epilepsy

Pediatric Neurology Briefs

Volume 15 (2001): Issue 10

By: J Gordon Millichap

Open Access

|Oct 2001

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.

References

Brockmann K Wang D Korenke CG von Moers A Ho YY Pascual JM Autosomal dominant glut-1 deficiency syndrome and familial epilepsy Ann Neurol 2001 Oct 50 4 476 85 10.1002/ana.1222 11603379
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-15-10-2 | Journal eISSN: 2166-6482

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Language: English

Page range: 74 - 75

Published on: Oct 1, 2001

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Deficiency Syndrome,

Antiepileptic Drugs,

Mild Ataxia-Dystonia

© 2001 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 15 (2001): Issue 10