RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164085863 T1 Sturge-Weber Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164085863 RD 2024/03/29 AB A neurocutaneous syndrome characterized by the presence of vascular tumors of the face (facial hemangioma and nevus flammeus, usually called “port-wine stain”), ipsilateral vascular anomalies (angioma of the meninges and choroid), and intracranial calcifications. Other clinical features include contralateral hemiparesis, hemianopia, and severe seizures. This nevus flammeus of the face corresponds to the ophthalmic division of the trigeminal nerve. All organs can be involved.