Sturge-Weber二氏综合征又名眼—神经—皮肤血管瘤病。近年来有称为三体型—22综合征。我们仍以惯称Sturge-Weber二氏综合征命名。该综合征具有颜面血管瘤、癫癎和青光眼三大特征,临床上常见为不完全型。由于本病的临床和病理改变与Von Recklinghausen病、结节性硬化症、Von Hippel病 Sturge-Weber’s syndrome, also known as ocular-neuro-cutaneous hemangiomatosis. In recent years there is known as trisomy-22 syndrome. We are still named after Sturge-Weber’s syndrome. The syndrome has facial hemangiomas, epilepsy and glaucoma three major features, clinically common incomplete type. Due to the clinical and pathological changes of the disease and Von Recklinghausen disease, tuberous sclerosis, Von Hippel disease