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黏多糖贮积病Ⅵ型合并虹膜睫状体囊肿和睫状体脱离一例 被引量:1

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摘要 黏多糖贮积病(mucopolysaccharidosis,MPS)是代谢黏多糖的溶酶体酶活性降低或缺乏造成的细胞内和细胞外黏多糖增多和分布异常,从而引起多器官的病变。根据血液酶学检查结果,可将MPS分为MPSI、MPSII(Hunter综合征)、MPSⅢ(Sanfilippo综合征)、MPSⅣ(Morquio综合征)、MPSVI(Maroteaux-Lamy综合征)、MPSVII(Sly综合征)、MPSⅨ(Natowicz综合征)等类型。
出处 《中华眼科杂志》 CAS CSCD 北大核心 2009年第11期1047-1049,共3页 Chinese Journal of Ophthalmology
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参考文献10

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同被引文献26

  • 1施惠平.溶酶体贮积症[J].实用儿科临床杂志,2007,22(8):561-563. 被引量:4
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