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原发性海蓝组织细胞增多症1例 被引量:3

原发性海蓝组织细胞增多症1例
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摘要 海蓝组织细胞增多症(Sea—bluehistiocytesvndrome,SBHsyndrome)是一种罕见的脂质代谢障碍疾病.我院近期诊断I例,现报道如下。
出处 《中国实用儿科杂志》 CSCD 北大核心 2013年第1期74-75,共2页 Chinese Journal of Practical Pediatrics
关键词 海蓝组织细胞增多症 脂类代谢异常 Sea-blue histiocyte syndrome (SBH syndrome) abnormal lipid metabolism
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参考文献10

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二级参考文献6

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共引文献6

同被引文献11

  • 1王建中,张时民,刘贵建,等.临床检验诊断学图谱[M].北京:人民卫生出版社,2012:596.
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  • 8Betul T, Mualla T, Fatma G. Sea-blue histioeytes in the bone marrow of a boy with sever congenital neutropenia assoiated with G6PC3 mutation[J]. Brihaem, 2014, 165(4):426.
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  • 10万楚成.实用血液病理论与研究[M].武汉:湖北科学技术出版社,2005.343.

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