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We experienced a case of Sturge-Weber Syndrome in 6 month old male.
The diagnosis was established by charecteristic features of Sturge-Weber Syndrome such as
facial port-wine nevus, focal seizure, hemiparesis, glaucoma and typical calcification & brain
atrophy as on brain CT. Plain radiographys of the skull revealed no evidence of calcification, But the brain C.T.
clearly showed calcific densities. We have presented this case... |
