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.
Andriola M, Stolfi J. Sturge-Weber Syndrome: Report of an Atypical Case. Am J Dis Child. 1972;123(5):507–510. doi:10.1001/archpedi.1972.02110110135019
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