Gupta Archana, Dubey Suneeta, Agarwal Manisha
Department of Paediatric Ophthalmology, Department of Glaucoma, Department of Vitreoretina, Dr. Shroff's Charity Eye Hospital, Daryaganj, New Delhi, India.
J AAPOS. 2007 Aug;11(4):398-9. doi: 10.1016/j.jaapos.2007.02.016. Epub 2007 May 23.
Sturge-Weber syndrome is a rare neurocutaneous disorder characterized by a facial nevus flammeus and extensive angiomatous changes involving the leptomeninges, the dura, and vessels of the gray and white matter. Oculodermal melanocytosis is characterized by hyperpigmentation of the facial skin in the distribution of the ophthalmic, maxillary, and occasionally mandibular division of the trigeminal nerve.
斯特奇-韦伯综合征是一种罕见的神经皮肤疾病，其特征为面部葡萄酒色斑以及累及软脑膜、硬脑膜和灰白质血管的广泛血管瘤样改变。眼皮肤黑素细胞增多症的特征是三叉神经眼支、上颌支分布区域，偶尔在下颌支分布区域的面部皮肤色素沉着。
