Sturge-Weber Syndrome: A Case Report

Journal Title: Scholars Journal of Applied Medical Sciences - Year 2017, Vol 5, Issue 8

Abstract

Abstract:Sturge-Weber syndrome (SWS) is a rare, congenital, neuro-oculo-cutaneous disorder which is characterized by port-wine stain (facial nevus), glaucoma, seizures, hemiparesis, intracranial calcification and mental retardation. In the present case, a 17-year-old male patient presented with a port wine stain on the left side of the face, glaucoma of the left eye, seizure and weakness of right sided weakness of body. Keywords:SWS - Sturge-Weber syndrome

Authors and Affiliations

Pradeep Nigam, Shivaji Thakare, Umesh Pratap Singh, Manoj Idurkar4

Keywords

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  • EP ID EP373000
  • DOI -
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How To Cite

Pradeep Nigam, Shivaji Thakare, Umesh Pratap Singh, Manoj Idurkar4 (2017). Sturge-Weber Syndrome: A Case Report. Scholars Journal of Applied Medical Sciences, 5(8), 3060-3064. https://europub.co.uk./articles/-A-373000