Thromb Haemost 1960; 4(03): 369-375
DOI: 10.1055/s-0038-1654520
Originalarbeiten — Original Articles — Travaux Originaux
Schattauer GmbH

Spontaneous Haemophilia in a Female

E. H Braun*
,
David B. Stollar**
Further Information

Publication History

Publication Date:
17 June 2018 (online)

Summary

A case of haemophilia in a young white girl is described. There was a history of bleeding from birth. The thromboplastin generation test was grossly abnormal and A. H. G. levels were below 1%. Bleeding time and capillary morphology was within normal limits. Dental extraction after transfusion caused almost uncontrollable haemorrhage.

A complete family history was obtained for four generations. There was no case of a “bleeder” amongst these.

The girl’s apparent sex was confirmed by sex chromatin studies.

* M.D. (Sask.), M. R. C. P. (Edin.), M. R. C. S. (Eng.), D. T. M. & H. (Liverpool). Assistant Pathologist, Pathology Dept., University Hospital, Saskatoon, Sask. Assistant Professor of Pathology, University of Saskatchewan, Saskatoon, Sask.


** B.A. (Sask.), M.D. (Sask.), University Hospital, Saskatoon.