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血小板無力症

維基百科,自由的百科全書
血小板冇力症
類型blood platelet disease[*]inherited blood coagulation disease[*]rare hemorrhagic disorder due to a qualitative platelet defect[*]疾病
分類和外部資源
醫學專科血液學
ICD-10D69.1
ICD-9-CM287.1
OMIM273800
DiseasesDB5224
MedlinePlus001305
eMedicine200311
Orphanet849
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血小板無力症 是一種極其罕見的血液疾病,原因是血小板缺乏糖蛋白IIb/IIIa受體(GPIIB/IIIA), 所以纖維蛋白原很難交聯,致使出血時間顯著延長。

病因學

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血小板無力症屬自體隱性遺傳[1],另亦可由自體免疫性疾病引致[2]

臨床特點

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參考文獻

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  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頁面存檔備份,存於網際網路檔案館).
  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.

參見

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