Kouskoukis C E, Kanitakis C J
J Dermatol Surg Oncol. 1982 Jan;8(1):47-50. doi: 10.1111/j.1524-4725.1982.tb00234.x.
The Sturge-Weber syndrome is a congenital anomaly that is characterized principally by unilateral angiomatosis of the skin, cerebral meninges and choroid of the eye. It may be attended by mental retardation, convulsions, hemiplegia, and visual disturbances. The complete syndrome is rare. We herewith report a case of the syndrome fairly fully developed.
斯特奇-韦伯综合征是一种先天性异常,主要特征为皮肤、脑膜和脉络膜单侧血管瘤病。可能伴有智力迟钝、惊厥、偏瘫和视觉障碍。完整的综合征较为罕见。我们在此报告一例该综合征充分发展的病例。