Sturge-Weber Syndrome with Port Wine Stain and Bilateral Choroid Plexus Angiomas: A Case Report

Sturge-Weber Syndrome with Port Wine Stain and Bilateral Choroid Plexus Angiomas: A Case Report

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...

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Veröffentlicht in:Journal of medicine 2014, Vol.15 (1), p.68-70
Hauptverfasser: Ahmad, Kaleem, Ansari, Sajid, Dhungel, Kanchan, Gupta, Mukesh Kumar, Pant, Ashok Raj, Rauniyar, R K
Format: Artikel
Sprache:eng
Schlagworte:
Clinical outcomes
Medical disorders
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Zusammenfassung: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
ISSN:1997-9797
2075-5384
DOI:10.3329/jom.v15i1.19877