[前列腺素系统缺陷。I. 家族性全血浆因子缺乏症]
[Defects in the prostaglandin system. I. Familial total plasma factor deficiency].
作者信息
Sinzinger H, Fitscha P
出版信息
Wien Klin Wochenschr. 1985 Jan 18;97(2):73-6.
PMID:3885578
Abstract
A case of a 38 year-old male is reported, in whom routine general investigation after myocardial infarction revealed a deficiency in the prostacyclin synthesis stimulating plasma factor. Examination of all available members of the family showed a congenital defect of as yet unknown pathogenetic significance.
摘要
报告了一例38岁男性病例，该患者心肌梗死后的常规全身检查显示前列环素合成刺激血浆因子缺乏。对该家族所有在世成员的检查显示出一种病因尚不明的先天性缺陷。
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