• 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

[安哥拉共和国的镰状细胞病。2. 实验室参数表现]

[Sickle cell disease in the People's Republic of Angola. 2. Behavior of laboratory parameters].

作者信息

Eggert W, Bernardino L, de Cruz M, Eggert S, Schmidt G

机构信息

Klinik und Poliklinik für Kinderheilkunde, Humboldt-Universität zu Berlin.

出版信息

Folia Haematol Int Mag Klin Morphol Blutforsch. 1987;114(6):866-73.

PMID:2453417
Abstract

In 819 children the Hb concentration, its dependence on the course of disease, the impact of various crises on Hb values and the behaviour of MCHC were evaluated. In the mean there was an anemia of 4.65 +/- 0.5 Hb mmol/l. In the course of 6 years a significant decline anemia of 4.65 +/- 0.5 Hb mmol/l. In the course of 6 years a significant decline of the Hb concentration could be observed. Only those crises connected with severe clinical symptoms (third degree) coincide with a significant Hb decrease. Every second child with a mean Hb value of 2.3 mml/l was transfused. In nearly half the cases there is a normochromic anemia, in 45.7% a hypochromic one. The mean serum bilirubin concentration lay at 31.6 mumol/l and increased with growing age of disease. The anemia has negative effects on the cardio-circulating system. The thorax-heart quotient shows a positive correlation to the degree of anemia.

摘要

对819名儿童的血红蛋白浓度、其与病程的关系、各种危象对血红蛋白值的影响以及平均红细胞血红蛋白浓度(MCHC)的变化情况进行了评估。平均血红蛋白浓度为4.65±0.5毫摩尔/升,存在贫血。在6年的病程中,可观察到血红蛋白浓度显著下降。只有那些伴有严重临床症状(三级)的危象才会导致血红蛋白显著降低。平均血红蛋白值为2.3毫摩尔/升的儿童中有一半接受了输血。近一半病例为正色素性贫血,45.7%为低色素性贫血。血清胆红素平均浓度为31.6微摩尔/升,并随病程延长而升高。贫血对心血管循环系统有负面影响。心胸比值与贫血程度呈正相关。

相似文献

1
[Sickle cell disease in the People's Republic of Angola. 2. Behavior of laboratory parameters].[安哥拉共和国的镰状细胞病。2. 实验室参数表现]
Folia Haematol Int Mag Klin Morphol Blutforsch. 1987;114(6):866-73.
2
[Sickle cell disease in the People's Republic of Angola. 1. Epidemiology and clinical aspects].[安哥拉共和国的镰状细胞病。1. 流行病学与临床方面]
Folia Haematol Int Mag Klin Morphol Blutforsch. 1987;114(6):857-65.
3
The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, beta-globin gene haplotype, co-inherited alpha-thalassemia trait and Hb F on steady-state serum bilirubin levels in sickle cell anemia.尿苷二磷酸葡萄糖醛酸基转移酶1A启动子多态性、β-珠蛋白基因单倍型、共同遗传的α-地中海贫血特征及胎儿血红蛋白对镰状细胞贫血患者稳态血清胆红素水平的影响
Eur J Haematol. 2005 Aug;75(2):150-5. doi: 10.1111/j.1600-0609.2005.00477.x.
4
Genetic Blood Disorders Survey in the Sultanate of Oman.阿曼苏丹国的遗传性血液疾病调查。
J Trop Pediatr. 2003 Jul;49 Suppl 1:i1-20.
5
[The status of hemoglobin concentration and hematocrit in Angola children].[安哥拉儿童的血红蛋白浓度和血细胞比容状况]
Kinderarztl Prax. 1992 Apr;60(2):49-53.
6
Hb F levels, longevity of homozygotes and clinical course of sickle cell anemia in Brazil.巴西的血红蛋白F水平、纯合子的寿命及镰状细胞贫血的临床病程
Am J Med Genet. 1983 Apr;14(4):669-76. doi: 10.1002/ajmg.1320140410.
7
Childhood deaths from anaemia in Accra, Ghana.加纳阿克拉儿童因贫血导致的死亡情况。
West Afr J Med. 1995 Apr-Jun;14(2):101-4.
8
Hemoglobin F concentration as a function of age in Kuwaiti sickle cell disease patients.科威特镰状细胞病患者血红蛋白F浓度与年龄的关系
Med Princ Pract. 2007;16(4):286-90. doi: 10.1159/000102151.
9
Overt iron deficiency in sickle cell disease.镰状细胞病中的明显缺铁
Arch Intern Med. 1982 Sep;142(9):1621-4.
10
Plasma fibrinogen levels in Nigerian homozygous (Hb SS) sickle cell patients.尼日利亚纯合子(Hb SS)镰状细胞病患者的血浆纤维蛋白原水平
Hemoglobin. 2007;31(1):89-92. doi: 10.1080/03630260601059217.