斯特格-韦伯综合征I型:一个罕见的病例报告
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
概括
这一案例记录了一种罕见的Sturge-Weber综合征 (SWS) 类型I, 早期诊断和治疗导致完全康复,强调SWS
科学领域:
- 神经皮肤疾病
- 血管疾病
- 神经学
背景情况:
- 斯特格-韦伯综合征 (SWS) 是一种罕见的先天性疾病,其特征是面部葡萄酒污点,膜血管瘤和眼部异常.
- SWS通常表现为神经缺陷,如和发育迟缓,通常与大脑的广泛参与有关.
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