ストルゲ・ウィーバー症候群 タイプI: 稀な症例報告
Batoul Hendieh1, Firas Khana2, Sevin Ibrahim1
1Department of Pediatrics, Faculty of Medicine, University of Aleppo, Aleppo University Hospital (AUH), Aleppo, Syria.
Annals of medicine and surgery (2012)
|September 3, 2025
まとめ
この症例は,急性神経学的症状を伴う ストルゲ・ウィーバー症候群 (SWS) タイプIの希少な症例を記録しています. 早期の診断と治療は完全回復につながり,SWSを強調しました.
科学分野:
- 神経皮質疾患
- 血管の異常
- 神経学
背景:
- ストルージ・ウィーバー症候群 (SWS) は,顔のポートワインの汚れ,レプトメニンゲアル血管腫,および眼異常によって特徴づけられる珍しい先天性疾患である.
- SWSは通常,発作や発達遅延などの神経学的欠陥を示し,しばしば広範な脳の関与と関連しています.
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