Sturge-Weber syndrome without port-wine facial nevus. Report of 2 cases studied by CT.

Child's brain Pub Date : 1983-01-01 DOI:10.1159/000120140
P Ambrosetto, G Ambrosetto, R Michelucci, A Bacci
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引用次数: 44

Abstract

2 cases of Sturge-Weber syndrome without facial nevus are reported. The patients presented different forms of epilepsy. The diagnosis was made by computed tomography (CT) which showed typical intracranial calcifications in both occipital regions. The problems concerning the atypical and incomplete forms of the syndrome are briefly discussed. The importance of CT as a diagnostic procedure for this disease is emphasized.

无葡萄酒面部痣的斯特奇-韦伯综合征。2例CT分析报告。
本文报告2例无面部痣的Sturge-Weber综合征。患者表现出不同形式的癫痫。计算机断层扫描(CT)显示典型的颅内钙化在两个枕区。关于非典型和不完全形式的综合征的问题进行了简要的讨论。强调了CT作为本病诊断手段的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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