{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,6]],"date-time":"2025-11-06T06:19:34Z","timestamp":1762409974468,"version":"build-2065373602"},"reference-count":13,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2025,11,5]]},"DOI":"10.7759\/cureus.96176","type":"journal-article","created":{"date-parts":[[2025,11,6]],"date-time":"2025-11-06T06:04:46Z","timestamp":1762409086000},"source":"Crossref","is-referenced-by-count":0,"title":["Not Just a Birthmark: A Case Report of a Subtle Port-Wine Stain Heralding Sturge-Weber Syndrome"],"prefix":"10.7759","author":[{"given":"Mohnish","family":"Darshan","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sabavath","family":"Arun","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Harshit","family":"Khandelwal","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Amber","family":"Kumar","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shikha","family":"Malik","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.2147\/TACG.S363685","article-title":"Sturge-Weber syndrome: a review of pathophysiology, genetics, clinical features, and current management approache","volume":"16","author":"S\u00e1nchez-Espino LF","year":"2023","unstructured":"S\u00e1nchez-Espino LF, Ivars M, Anto\u00f1anzas J, Baselga E. Sturge-Weber syndrome: a review of pathophysiology, genetics, clinical features, and current management approache. Appl Clin Genet. 2023, 16:63-81. 10.2147\/TACG.S363685","journal-title":"Appl Clin Genet"},{"key":"ref2","article-title":"Sturge Weber syndrome - a case report","volume":"3","author":"Patil K","year":"2015","unstructured":"Patil K, Guledgud MV, Sahni A. Sturge Weber syndrome - a case report. Int J Dent Sci Res. 2015, 3:45-7.","journal-title":"Int J Dent Sci Res"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.31729\/jnma.8344","article-title":"Sturge-Weber syndrome: a case report","volume":"61","author":"Timilsina S","year":"2023","unstructured":"Timilsina S, Kunwor B, Thapa Chhetri S, Nepal S, Sedhai K. Sturge-Weber syndrome: a case report. JNMA J Nepal Med Assoc. 2023, 61:890-2. 10.31729\/jnma.8344","journal-title":"JNMA J Nepal Med Assoc"},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.1016\/j.pediatrneurol.2021.04.013","article-title":"Consensus statement for the management and treatment of Sturge-Weber syndrome: neurology, neuroimaging, and ophthalmology recommendations","volume":"121","author":"Sabeti S","year":"2021","unstructured":"Sabeti S, Ball KL, Bhattacharya SK, et al.. Consensus statement for the management and treatment of Sturge-Weber syndrome: neurology, neuroimaging, and ophthalmology recommendations. Pediatr Neurol. 2021, 121:59-66. 10.1016\/j.pediatrneurol.2021.04.013","journal-title":"Pediatr Neurol"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.11604\/pamj.2020.36.273.24346","article-title":"Sturge-Weber syndrome: about a case (Article in French)","volume":"36","author":"Doumiri M","year":"2020","unstructured":"Doumiri M, Labied M, Salam S, Laoudiyi D, Chbani K, Ouzidane L. Sturge-Weber syndrome: about a case (Article in French). Pan Afr Med J. 2020, 36:273. 10.11604\/pamj.2020.36.273.24346","journal-title":"Pan Afr Med J"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.4081\/mi.2013.e7","article-title":"Sturge-weber syndrome: a report of 14 cases","volume":"5","author":"Parisi L","year":"2013","unstructured":"Parisi L, Di Filippo T, La Grutta S, et al.. Sturge-weber syndrome: a report of 14 cases. Ment Illn. 2013, 5:e7. 10.4081\/mi.2013.e7","journal-title":"Ment Illn"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.2147\/IMCRJ.S472356","article-title":"An atypical seizure onset and re-emergence in a refugee with an undiagnosed Sturge-Weber syndrome: a case report from a limited setting","volume":"17","author":"Saad AH","year":"2024","unstructured":"Saad AH, Omar SM, Elgilli AA, Omer IA, Jalaleldeen MH. An atypical seizure onset and re-emergence in a refugee with an undiagnosed Sturge-Weber syndrome: a case report from a limited setting. Int Med Case Rep J. 2024, 17:615-20. 10.2147\/IMCRJ.S472356","journal-title":"Int Med Case Rep J"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.1016\/j.jpeds.2019.08.025","article-title":"Sturge-Weber syndrome patient registry: delayed diagnosis and poor seizure control","volume":"215","author":"Cho S","year":"2019","unstructured":"Cho S, Maharathi B, Ball KL, Loeb JA, Pevsner J. Sturge-Weber syndrome patient registry: delayed diagnosis and poor seizure control. J Pediatr. 2019, 215:158-63. 10.1016\/j.jpeds.2019.08.025","journal-title":"J Pediatr"},{"key":"ref9","doi-asserted-by":"publisher","DOI":"10.4103\/0972-2327.107725","article-title":"A clinician's dilemma: Sturge-Weber syndrome 'without facial nevus'!!","volume":"16","author":"Jagtap SA","year":"2013","unstructured":"Jagtap SA, Srinivas G, Radhakrishnan A, Harsha KJ. A clinician's dilemma: Sturge-Weber syndrome 'without facial nevus'!!. Ann Indian Acad Neurol. 2013, 16:118-20. 10.4103\/0972-2327.107725","journal-title":"Ann Indian Acad Neurol"},{"key":"ref10","doi-asserted-by":"publisher","DOI":"10.4274\/jpr.44265","article-title":"Sturge-Weber syndrome type III","volume":"5","author":"Tekin HG","year":"2018","unstructured":"Tekin HG, G\u00f6kben S, Y\u0131lmaz S, et al.. Sturge-Weber syndrome type III. J Pediatr Res. 2018, 5:103-5. 10.4274\/jpr.44265","journal-title":"J Pediatr Res"},{"key":"ref11","doi-asserted-by":"publisher","DOI":"10.1186\/s12883-020-01944-5","article-title":"Isolated leptomeningeal angiomatosis in the sixth decade of life, an adulthood variant of Sturge Weber Syndrome (Type III): role of advanced Magnetic Resonance Imaging and Digital Subtraction Angiography in diagnosis","volume":"20","author":"Muralidharan V","year":"2020","unstructured":"Muralidharan V, Failla G, Travali M, Cavallaro TL, Politi MA. Isolated leptomeningeal angiomatosis in the sixth decade of life, an adulthood variant of Sturge Weber Syndrome (Type III): role of advanced Magnetic Resonance Imaging and Digital Subtraction Angiography in diagnosis. BMC Neurol. 2020, 20:366. 10.1186\/s12883-020-01944-5","journal-title":"BMC Neurol"},{"key":"ref12","article-title":"MR and MR angiography of Sturge-Weber syndrome","volume":"14","author":"Vogl TJ","year":"1993","unstructured":"Vogl TJ, Stemmler J, Bergman C, Pfluger T, Egger E, Lissner J. MR and MR angiography of Sturge-Weber syndrome. AJNR Am J Neuroradiol. 1993, 14:417-25.","journal-title":"AJNR Am J Neuroradiol"},{"key":"ref13","doi-asserted-by":"publisher","DOI":"10.1089\/lrb.2007.1016","article-title":"Update on Sturge-Weber syndrome: diagnosis, treatment, quantitative measures, and controversies","volume":"5","author":"Comi AM","year":"2007","unstructured":"Comi AM. Update on Sturge-Weber syndrome: diagnosis, treatment, quantitative measures, and controversies. Lymphat Res Biol. 2007, 5:257-64. 10.1089\/lrb.2007.1016","journal-title":"Lymphat Res Biol"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/408594-not-just-a-birthmark-a-case-report-of-a-subtle-port-wine-stain-heralding-sturge-weber-syndrome","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,11,6]],"date-time":"2025-11-06T06:04:48Z","timestamp":1762409088000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/408594-not-just-a-birthmark-a-case-report-of-a-subtle-port-wine-stain-heralding-sturge-weber-syndrome"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,11,5]]},"references-count":13,"URL":"https:\/\/doi.org\/10.7759\/cureus.96176","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2025,11,5]]}}}