血小板无力症

血小板无力症 是一种极其罕见的血液疾病，原因是血小板缺乏糖蛋白IIb/IIIa受体(GPIIB/IIIA), 所以纤维蛋白原很难交联，致使出血时间显著延长。

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血小板冇力症
类型blood platelet disease[*]、inherited blood coagulation disease[*]、rare hemorrhagic disorder due to a qualitative platelet defect[*]、疾病
分类和外部资源
醫學專科血液學
ICD-10D69.1
ICD-9-CM287.1
OMIM273800
DiseasesDB5224
MedlinePlus001305
eMedicine200311
Orphanet849

病因学

血小板无力症屬自體隱性遺傳[1]，另亦可由自體免疫性疾病引致[2]。

临床特点

参考文献
  1. Seligsohn U. Glanzmann thrombasthenia: a model disease which paved the way to powerful therapeutic agents. Pathophysiol Haemost Thromb. 2002 Sep-Dec;32(5-6):216-7. PMID 13679645. Free Full Text （页面存档备份，存于）.
  2. Tholouli E, Hay CR, O'Gorman P, Makris M. Acquired Glanzmann's thrombasthenia without thrombocytopenia: a severe acquired autoimmune bleeding disorder. Br J Haematol. 2004 Oct;127(2):209-13. PMID 15461628.

参见
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