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  Vol. 123 No. 5, May 1972 TABLE OF CONTENTS
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Sturge-Weber Syndrome

Report of an Atypical Case

Mary Andriola, MD; Joseph Stolfi, MD

Am J Dis Child. 1972;123(5):507-510.


Abstract

A patient had Sturge-Weber syndrome without the characteristic facial nevus or mental retardation. Abnormal findings included seizures, typical intracranial calcifications in the parietooccipital area, and a homonymous hemianopsia.



Author Affiliations

New Orleans

From the Department of Neurology, Louisiana State University School of Medicine, New Orleans.


Footnotes

Received for publication Oct 18, 1971; accepted Dec 28.

Reprint requests to 1542 Tulane Ave, New Orleans 70112 (Dr. Andriola).



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Familial occipital calcifications, hemorrhagic strokes, leukoencephalopathy, dementia, and external carotid dysplasia
Iglesias et al.
Neurology 2000;55:1661-1667.
ABSTRACT | FULL TEXT  





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