A CASE OF CONGENITAL DEFICIENCY OF FACTOR X (STUART-PROWER)

被引：4

作者：

SZONYI, L

PALOS, T

RENTKA, M

机构：

来源：

ZEITSCHRIFT FUR KINDERHEILKUNDE | 1969年 / 106卷 / 02期

关键词：

D O I：

10.1007/BF00476250

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

The authors give the case history of a girl suffering from factor X deficiency. The importance of factor X in blood coagulation, and the diagnostic laboratory methods used are discussed. This is the first case of a factor X deficiency observed in Hungary. © 1969 Springer-Verlag.

引用

页码：100 / &

共 16 条

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BACHMANN F, 1957, THROMB DIATH HAEMOST, V1, P169

[2]

BARKAGAN ZS, 1965, KLIN MED MOSCOW, V43, P120

[3]

FISCH U, 1959, THROMB DIATH HAEMOST, V3, P98

[4]

GERENDAS M, 1960, BLUTUNG BLUTSTILLUNG

[5] STUART CLOTTING DEFECT .2. GENETIC ASPECTS OF A NEW HEMORRHAGIC STATE [J].