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CASE REPORT
Year : 2020  |  Volume : 32  |  Issue : 3  |  Page : 303-307

Birthmark: Journey from aesthetic to unalluring


1 Department of Oral Medicine and Radiology, RKDF Dental College and Research Centre, Bhopal, Madhya Pradesh, India
2 Department of Oral and Maxillofacial Surgery, Index Institute of Dental Sciences, Indore, Madhya Pradesh, India

Correspondence Address:
Dr. Sakshi Sharma
Flat No -103, RKDF Campus, SRK University, NH-12 Misrod, Bhopal, Madhya Pradesh - 462 026
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jiaomr.jiaomr_9_20

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Encephalotrigeminal Angiomatosis, also known as Sturge Weber Syndrome (SWS), Dimitri disease, Sturge Kalischer Weber Syndrome is specifically non familial, congenital rare disorder consisting of hamartomatous malformations that may affect eye, skin, and CNS. Failure of proper vascular development is believed to be the most likely cause of the condition. The malformed blood vessels may lead to port wine stains, epilepsy, and glaucoma depending on its location. We are presenting here a triad of case reports on Sturge Weber Syndrome representing individuals belonging to varied age groups.


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