• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[Diagnosis of hemolytic anemia with unstable hemoglobin].

作者信息

Sakalová A, Hrubisko M

出版信息

Folia Haematol Int Mag Klin Morphol Blutforsch. 1980;107(4):641-7.

PMID:6162731
Abstract

Heinz-body haemolytic anaemia represents a rarely occurring kind of hereditary defect of haemoglobin, G-6-PDH or glutathion reductase. The course of disease observed in two patients with non-spherocytic haemolytic anaemia was very serious as compared with other cases with haemoglobin variants and enzyme defects of G-6-PDH described in literature. The course of disease could not be influenced by splenectomy, substitution therapy, and long-term therapy with desferrioxamin. Exitus occurred at an age 22 or 41 as a consequence of severe haemosiderosis.

摘要

相似文献

1
[Diagnosis of hemolytic anemia with unstable hemoglobin].
Folia Haematol Int Mag Klin Morphol Blutforsch. 1980;107(4):641-7.
2
[Heinz bodies in non-spherocytic congenital hemolytic anemia].
Minerva Pediatr. 1968 Dec 22;20(51):2688-91.
3
Familial haemolytic anaemia with erythrocyte inclusion bodies, bilifuscinuria and abnormal haemoglobin (haemoglobin Galliera Genova).
Br J Haematol. 1965 Sep;11(5):511-7. doi: 10.1111/j.1365-2141.1965.tb00095.x.
4
THE HEREDITARY NON-SPHEROCYTIC HAEMOLYTIC ANAEMIAS.遗传性非球形细胞溶血性贫血
Acta Haematol. 1964 Apr;31:177-86. doi: 10.1159/000209626.
5
CONGENITAL HEINZ-BODY ANAEMIA. FURTHER EVIDENCE ON THE CAUSE OF HEINZ-BODY PRODUCTION IN RED CELLS.先天性海因茨小体细胞贫血。关于红细胞中海因茨小体产生原因的进一步证据。
Br J Haematol. 1964 Jul;10:281-90. doi: 10.1111/j.1365-2141.1964.tb00704.x.
6
Inherited, non-spherocytic haemolysis due to deficiency of glucose-6-phosphate dehydrogenase.葡萄糖-6-磷酸脱氢酶缺乏所致的遗传性非球形红细胞性溶血
Scand J Clin Lab Invest. 2007;67(1):105-11. doi: 10.1080/00365510601047910.
7
Hereditary non-spherocytic haemolytic anaemia with post-splenectomy inclusion bodies and pigmenturia caused by an unstable haemoglobin Santa Ana-beta-88 (F4) leucine--proline.遗传性非球形细胞溶血性贫血,伴有脾切除术后包涵体和色素尿,由不稳定血红蛋白圣安娜-β-88(F4)亮氨酸-脯氨酸引起。
J Med Genet. 1968 Dec;5(4):292-7. doi: 10.1136/jmg.5.4.292.
8
[Pyrimidine 5'-nucleotidase deficiency as the congenital cause of nonspherocytic hemolytic anemia].[嘧啶5'-核苷酸酶缺乏作为非球形红细胞溶血性贫血的先天性病因]
Dtsch Med Wochenschr. 1993 Sep 10;118(36):1276-80. doi: 10.1055/s-2008-1059451.
9
[Enzyme deficient non-spherocytic hemolytic anemias].[酶缺乏性非球形红细胞溶血性贫血]
Z Gesamte Inn Med. 1978 May 1;33(9):276-82.
10
[Red cell enzyme deficiencies - clinical manifestation and pathophysiology (author's transl)].红细胞酶缺乏症——临床表现与病理生理学(作者译)
Monatsschr Kinderheilkd. 1981 Aug;129(8):444-53.