Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3157519 | Journal of Oral Biology and Craniofacial Research | 2015 | 4 Pages |
Abstract
Sturge–Weber syndrome (SWS), also called as encephalotrigeminal angiomatosis is an uncommon congenital neurological disorder & frequent among the neurocutaneous syndromes specifically with vascular predominance. This disorder is characterized by facial capillary malformation & other neurological condition. The oral manifestations are gingival hemangiomatosis restricting to either side in upper and lower jaw, sometimes bilateral. We report a case of SWS with oral, ocular and neurological features.
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Authors
Shahid M. Shaikh, Mousumi Goswami, Sanjay Singh, Darrel Singh,