TY - JOUR T1 - A girl with Sturge Weber syndrome and oro – maxillo -facial osteodystrophy TT - معرفی دختر مبتلا به سندرم استورج وبر همراه با بدشکلی استخوانی در ناحیه دهان- فک بالا- صورت JF - Yafteh JO - Yafteh VL - 16 IS - 3 UR - http://yafte.lums.ac.ir/article-1-1750-en.html Y1 - 2015 SP - 112 EP - 117 KW - Syndrome KW - Sturge -Weber KW - seizure KW - osteodystrophy. N2 - Background: Sturge-Weber syndrome is one of the rare neurocutaneous disorders with frequency of approximately 1 per 50,000. Sturge-Weber syndrome consists of a constellation of symptoms and signs including a facial nevus (port wine stain), seizure and hemiparesis. In many cases it may associate with mental retardation. Case presentation: A 7- year old girl with mental retardation and a large facial nevus at the birth time, recurrent severe seizures and drolling in 9 months of life without any treatment, was admitted because of severity of seizure, headache and weakness. Conducted follow up on here, indicated that she had Sturge –Weber syndrome with oro- maxilla -facial osteodystrophy. Conclusion: One of the rare radiological symptoms in Sturge Weber syndrome is oro-maxillo-facial osteodystrophy, by this time only few cases had been reported. All of the symptoms of this syndrome were found in our described patient M3 ER -