4.2 Review

Thrombotic thrombocytopenic purpura: A thrombotic disorder caused by ADAMTS 13 deficiency

期刊

出版社

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.hoc.2007.06.003

关键词

-

资金

  1. NHLBI NIH HHS [R01 HL062136-08, HL62136, R01 HL062136] Funding Source: Medline

向作者/读者索取更多资源

A serious disorder with characteristic microvascular thrombosis involving the brain and other organs, thrombotic thrombocytopenic purpura (TTP) typically presents with thrombocytopenia, hemolysis with schistocytes on blood smears, and mental changes or seizures. It may progress rapidly to a fatal end if the patient is not treated immediately with plasma. Recent advances have shown that TTP is caused by deficiency of a circulating, von Willebrand factor cleaving metalloprotease, ADAMTS13. This new knowledge will provide clues to improve the diagnosis and management of this intriguing disease.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.2
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据