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先天性红细胞生成异常性贫血Ⅱ型1例 被引量:1

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摘要 1.5岁男孩,面色苍白18个月,生后3d出现皮肤、巩膜黄染,尿呈黄色,大便不发白,黄疸时轻时重,双亲非近亲婚配,但有血缘关系。体检 面色苍黄,轻度方颅,前囱1cm×1cm,巩膜轻度黄染,口唇苍白,心尖部闻Ⅱ级收缩期吹风样杂音,肝右肋下2cm,脾左肋下3cm,质中等偏硬。末梢血RBC2×10<sup>12</sup>/L,血红蛋白50g/L,红细胞压积0.16,肝功正常。
机构地区 解放军
出处 《实用儿科临床杂志》 CAS CSCD 1993年第S1期61-61,共1页 Journal of Applied Clinical Pediatrics
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  • 1李津婴,许燕群,黄正霞,周虹,万树栋.Ⅱ型先天性红细胞生成异常性贫血患者红细胞膜超微结构和膜蛋白变化[J].中华内科杂志,2004,43(6):426-428. 被引量:5
  • 2陈英,张国平,曹励之,谢岷.两同胞兄弟共患先天性红细胞生成异常性贫血[J].中华儿科杂志,2005,43(12):944-945. 被引量:2
  • 3刘源,刘琼,原平飞,范淑兰,马宏,阴怀清.先天性红细胞生成异常性贫血1例(附文献复习)[J].山西医科大学学报,2006,37(7):770-773. 被引量:1
  • 4HEIMPEI. H, MATUSCHEK A,AHMEI) M,et al. Frequency of congenital dyserythropoietic anemias in Europe[J]. Eur J Haematol,2010.85:20--25.
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  • 7KAWABATA H. IDOISAKI S. OKAMOTO A. el al. A case of congenital dyserylhropoietic anemia type 1 in a Jap~mese aduh with a CDAN1 gene mulalion and an inappropriately low serum hepcidin-25 level[J]. In- tern Med,2012.51:917--920.
  • 8RUSSO R, GAMBALE A, ESPOSITO M R. et al. Two founder mulalions in the SE(?23B gene account for the relatively high frequency of CDA II in the ]tal-Am J Hematol, 2011, 86:727 -- 732.
  • 9LIU G,NIU S,DONG A,et al. A Chinese family car- rying novel mutations in SEC23B and HFE2, the genes responsible for congenital dyserythropoietic a naemia II (CDA II) and primary iron overload, respec tively[J]. Br J Haematol, 2012,158 : 143-- 145.
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