Sturge-Weber Syndrome with Port Wine Stain and Bilateral Choroid Plexus Angiomas: A Case Report
DOI:
https://doi.org/10.3329/jom.v15i1.19877Keywords:
Sturge-Weber Syndrome, Phakomatosis, Neurocutaneous Syndrome, Computed tomographyAbstract
Sturge-Weber syndrome is a rarenon-hereditary condition characterized by a hamartomatous vascular proliferation. It is usually unilateral; bilateral involvement is seen only in 15% cases. We report a case of a 6 month old male child with Sturge-Weber syndrome with its inherent clinical features and typical imaging findings.
DOI: http://dx.doi.org/10.3329/jom.v15i1.19877
J Medicine 2014; 15: 68-70
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Published
2014-08-06
How to Cite
Ahmad, K., Ansari, S., Dhungel, K., Gupta, M. K., Pant, A. R., & Rauniyar, R. K. (2014). Sturge-Weber Syndrome with Port Wine Stain and Bilateral Choroid Plexus Angiomas: A Case Report. Journal of Medicine, 15(1), 68–70. https://doi.org/10.3329/jom.v15i1.19877
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Case Reports
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