Suppr超能文献

与红细胞钠钾ATP酶活性正常水平相关的遗传性口形红细胞增多症家族。

A family of hereditary stomatocytosis associated with normal level of Na+-K+-ATPase activity of red blood cells.

作者信息

Mutoh S, Sasaki R, Takaku F, Aoyama M, Moriyama S, Yoshimoto M, Yawata Y

出版信息

Am J Hematol. 1983 Apr;14(2):113-20. doi: 10.1002/ajh.2830140203.

Abstract

A rare familial case of hereditary stomatocytosis with hemolytic anemia, increased autohemolysis, increased osmotic fragility, and shortened erythrocyte survival is described. The erythrocytes were abnormally permeable to sodium and potassium. In addition, "Na-K pump" rate of the red blood cells was increased, while Na+-K+-ATPase, Mg2+-ATPase and Mg2+-Ca2+-ATPase activities were within normal limits. Splenectomy induced marked improvement of anemia.

摘要

描述了一例罕见的家族性遗传性口形红细胞增多症病例,伴有溶血性贫血、自身溶血增加、渗透脆性增加和红细胞存活期缩短。红细胞对钠和钾的通透性异常。此外,红细胞的“钠-钾泵”速率增加,而钠钾ATP酶、镁ATP酶和镁钙ATP酶活性在正常范围内。脾切除术后贫血明显改善。

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