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  Vol. 38 No. 4, April 1981 TABLE OF CONTENTS
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  CHILD NEUROLOGY
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Moyamoya Disease in a Patient With Type I Glycogenosis

LCDR Theodore R. Sunder, MC

Arch Neurol. 1981;38(4):251-253.


Abstract

• A 17-year-old boy with type I glycogen storage disease (GSD-I) and a stroke associated with moyamoya disease is described. This is the first report of this association, and only the second reported case of cerebrovascular disease in patients with GSD-I. The relationship of the primary metabolic error and the vascular injury is explored. This represents yet another disorder associated with moyamoya disease, which is considered to be a secondary phenomenon of vascular occlusion that occurs under a specific set of circumstances in a susceptible age group.



Author Affiliations

USN

From the Department of Neurology, National Naval Medical Center, and the Department of Neurology, Uniformed Services University of the Health Sciences, Bethesda, Md.


Footnotes

Accepted for publication Aug 4, 1980.

The views expressed herein are those of the author and should not be construed as official or as necessarily reflecting the views of the National Naval Medical Center, the Uniformed Services University of the Health Sciences, or the Navy Medical Department.

Reprint requests to Department of Neurology, National Naval Medical Center, Bethesda, MD 20014 (Dr Sunder).



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Modified Encephaloduroarteriosynangiosis as a Surgical Treatment of Childhood Moyamoya Disease: Report of Five Cases
Rooney et al.
J Child Neurol 1991;6:24-31.
ABSTRACT  





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