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Sturge-Weber syndrome with port wine stain and bilateral choroid plexus angiomas: A case report
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نویسنده
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ahmad k. ,ansari s. ,dhungel k. ,gupta m.k. ,pant a.r. ,rauniyar r.k.
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منبع
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journal of medicine (bangladesh) - 2014 - دوره : 15 - شماره : 1 - صفحه:68 -70
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چکیده
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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.
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کلیدواژه
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Computed tomography; Neurocutaneous syndrome; Phakomatosis; Sturge-Weber syndrome
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آدرس
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department of radiodiagnosis,b.p. koirala institute of health sciences, Nepal, department of radiodiagnosis,b.p. koirala institute of health sciences, Nepal, department of radiodiagnosis,b.p. koirala institute of health sciences, Nepal, department of radiodiagnosis,b.p. koirala institute of health sciences, Nepal, department of radiodiagnosis,b.p. koirala institute of health sciences, Nepal, department of radiodiagnosis,b.p. koirala institute of health sciences, Nepal
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Authors
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