| Literature DB >> 25853049 |
Shahid M Shaikh1, Mousumi Goswami2, Sanjay Singh3, Darrel Singh4.
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.Entities:
Keywords: Gingival enlargement; Port-wine stains; Sturge–Weber syndrome
Year: 2015 PMID： 25853049 PMCID： PMC4382502 DOI： 10.1016/j.jobcr.2015.01.002
Source DB: PubMed Journal: J Oral Biol Craniofac Res ISSN： 2212-4268