{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,8,27]],"date-time":"2025-08-27T11:10:05Z","timestamp":1756293005844,"version":"3.44.0"},"reference-count":5,"publisher":"BMJ","content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["BMJ Case Reports"],"accepted":{"date-parts":[[2017,9,20]]},"abstract":"<jats:p>Sturge Weber syndrome also known as mother spot disease belongs to a group of disorders called phakomatoses (neurocutaneous syndromes involving the central nervous and cutaneous systems). It is a congenital disorder of the vasculature of the meninges, brain, face and eyes. Clinically, it usually presents with seizures and other neurological complications, including mental retardation, contralateral hemiparesis and glaucoma. Its incidence is estimated at one case in 20\u2009000\u201350 000 persons with equal frequency in boys and girls. We present a case of 18-months-old boy was brought by parents with history of seizures since birth resulting in fall 1\u2009day back. Physical examination showed bilateral port-wine stain on face. CT head examination revealed bilateral intracranial calcification. This is a highly unusual presentation of Sturge Weber syndrome.<\/jats:p>","DOI":"10.1136\/bcr-2017-219985","type":"journal-article","created":{"date-parts":[[2017,10,4]],"date-time":"2017-10-04T07:25:28Z","timestamp":1507101928000},"page":"bcr-2017-219985","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":1,"title":["Bilateral intracranial calcifications with bilateral facial cutaneous naevus: Sturge Weber syndrome"],"prefix":"10.1136","volume":"2017","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-4635-4448","authenticated-orcid":false,"given":"Muhammad Arif","family":"Saeed","sequence":"first","affiliation":[{"name":"Department of Radiology, Aga Khan University, Karachi, Pakistan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kiran","family":"Hilal","sequence":"additional","affiliation":[{"name":"Department of Radiology, Aga Khan University, Karachi, Pakistan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Prem","family":"Chand","sequence":"additional","affiliation":[{"name":"Department of Pediatrics and Child Health, Aga Khan University Hospital, Karachi, Pakistan"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[2017,10,4]]},"reference":[{"key":"2025082703344417000_2017.oct03_1.bcr-2017-219985.1","doi-asserted-by":"crossref","first-page":"407","DOI":"10.1016\/j.ad.2016.09.022","article-title":"Sturge-weber syndrome: a review","volume":"108","author":"Higueros","year":"2017","journal-title":"Actas Dermosifiliogr"},{"key":"2025082703344417000_2017.oct03_1.bcr-2017-219985.2","doi-asserted-by":"crossref","first-page":"257","DOI":"10.1016\/j.ejpn.2013.10.003","article-title":"Sturge-Weber syndrome: from the past to the present","volume":"18","author":"Sudarsanam","year":"2014","journal-title":"Eur J Paediatr Neurol"},{"key":"2025082703344417000_2017.oct03_1.bcr-2017-219985.3","doi-asserted-by":"publisher","DOI":"10.1136\/jnnp.39.5.429"},{"key":"2025082703344417000_2017.oct03_1.bcr-2017-219985.4","doi-asserted-by":"crossref","first-page":"323","DOI":"10.1542\/peds.87.3.323","article-title":"Location of port-wine stains and the likelihood of ophthalmic and\/or central nervous system complications","volume":"87","author":"Tallman","year":"1991","journal-title":"Pediatrics"},{"key":"2025082703344417000_2017.oct03_1.bcr-2017-219985.5","doi-asserted-by":"publisher","DOI":"10.2214\/ajr.158.4.1546607"}],"container-title":["BMJ Case Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/bcr-2017-219985","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,8,27]],"date-time":"2025-08-27T10:34:54Z","timestamp":1756290894000},"score":1,"resource":{"primary":{"URL":"https:\/\/casereports.bmj.com\/lookup\/doi\/10.1136\/bcr-2017-219985"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,10,4]]},"references-count":5,"alternative-id":["10.1136\/bcr-2017-219985"],"URL":"https:\/\/doi.org\/10.1136\/bcr-2017-219985","relation":{},"ISSN":["1757-790X"],"issn-type":[{"type":"electronic","value":"1757-790X"}],"subject":[],"published":{"date-parts":[[2017,10,4]]}}}