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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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