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婴儿型Aicardi-Goutières综合征1例病例报告及文献回顾 被引量:4

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摘要 1984年,Aicardi等。报道了来自5个家庭中的8个儿童主要表现为基底节钙化、脑白质异常和脑脊液淋巴细胞增多的进行性脑病,其后被定名为Aicardi Goutieres综合征(Aicardi—Goutieres syndrome,AGS)。
出处 《中国儿童保健杂志》 CAS 2017年第5期536-538,共3页 Chinese Journal of Child Health Care
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