DOI: 10.36347/sjams.2017.v5i08.020

Pages: 3060-3064

Sturge-Weber syndrome (SWS) is a rare, congenital, neuro-oculo-cutaneous disorder which is characterized by port-wine stain (facial nevus), glaucoma, seizures, hemiparesis, intracranial calcification and mental retardation. In the present case, a 17-year-old male patient presented with a port wine stain on the left side of the face, glaucoma of the left eye, seizure and weakness of right sided weakness of body.