发作作为Sturge-Weber综合征III型的初始症状:报告了两个病例
Yaping Wang1, Guifu Geng1, Wandong Hu1
1Epilepsy Center, Jinan Children's Hospital (Children's Hospital Affiliated to Shandong University), Jinan, Shandong 250000, P.R. China.
Experimental and therapeutic medicine
|June 13, 2024
概括
斯图尔奇-韦伯综合征 (SWS) 类型III是一种罕见的神经皮肤疾病,具有诊断挑战. 这项研究详细介绍了两个儿科病例,突出了和半等关键症状,以及改善预后的有效管理策略.
科学领域:
- 神经学 神经学
- 遗传学 是一个遗传学.
- 皮肤病学 皮肤病学
背景情况:
- 斯特-韦伯综合征 (SWS) 类型III是一种罕见的神经皮肤疾病.
- 由于可变的临床表现,它带来了重大的诊断挑战.
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