{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,13]],"date-time":"2026-10-13T00:01:17Z","timestamp":1791849677668,"version":"4.3.4"},"reference-count":6,"publisher":"BMJ","content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["BMJ Case Reports"],"accepted":{"date-parts":[[2015,2,19]]},"abstract":"<jats:p>Sturge-Weber syndrome is a rare, congenital, neuro-oculo-cutaneous disorder which is characterised extra-orally by unilateral port wine stains on the face, glaucoma, seizures and mental retardation, and intra-orally by ipsilateral gingival haemangioma which frequently affects the maxilla or mandible. In the present case, a 15-year-old female patient presented with a port wine stain on the right side of the face and glaucoma of the right eye, and intra-orally with gingival haemangioma on the right side of the maxilla.<\/jats:p>","DOI":"10.1136\/bcr-2014-207663","type":"journal-article","created":{"date-parts":[[2015,3,12]],"date-time":"2015-03-12T14:07:53Z","timestamp":1426169273000},"page":"bcr2014207663","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":19,"title":["Sturge-Weber syndrome: oral and extra-oral manifestations"],"prefix":"10.1136","volume":"2015","author":[{"given":"Amitandra Kumar","family":"Tripathi","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Vivek","family":"Kumar","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rahul","family":"Dwivedi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Charanjit Singh","family":"Saimbi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"239","published-online":{"date-parts":[[2015,3,12]]},"reference":[{"key":"2025042705414850000_2015.mar12_1.bcr2014207663.1","doi-asserted-by":"publisher","DOI":"10.1016\/0030-4220(66)90429-4"},{"key":"2025042705414850000_2015.mar12_1.bcr2014207663.2","first-page":"565","article-title":"Clinical features of Sturge-Weber syndrome","volume":"12","author":"Neto","year":"2008","journal-title":"Intl Arch Otorhinolaryngol"},{"key":"2025042705414850000_2015.mar12_1.bcr2014207663.3","doi-asserted-by":"publisher","DOI":"10.1891\/0730-0832.25.2.89"},{"key":"2025042705414850000_2015.mar12_1.bcr2014207663.4","doi-asserted-by":"publisher","DOI":"10.4103\/0970-4388.40319"},{"key":"2025042705414850000_2015.mar12_1.bcr2014207663.5","doi-asserted-by":"publisher","DOI":"10.1016\/S0387-7604(98)00067-9"},{"key":"2025042705414850000_2015.mar12_1.bcr2014207663.6","unstructured":"Del Monte M , Eisbschitz-Tsimhoni M . Sturge-Weber syndrome: overview. eMedicine February, 2007."}],"container-title":["BMJ Case Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/bcr-2014-207663","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,4,27]],"date-time":"2025-04-27T12:41:59Z","timestamp":1745757719000},"score":1,"resource":{"primary":{"URL":"https:\/\/casereports.bmj.com\/lookup\/doi\/10.1136\/bcr-2014-207663"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,3,12]]},"references-count":6,"alternative-id":["10.1136\/bcr-2014-207663"],"URL":"https:\/\/doi.org\/10.1136\/bcr-2014-207663","relation":{},"ISSN":["1757-790X"],"issn-type":[{"value":"1757-790X","type":"electronic"}],"subject":[],"published":{"date-parts":[[2015,3,12]]}}}