We describe a patient diagnosed in the neonatal period as having factor XIII deficiency who presented with persistent umbilical bleeding. Factor XIII deficiency is the only coagulation factor deficiency that cannot be detected by classical hemostatic tests, and a rapid diagnosis is vital during the first decade of life. A newborn presenting with persistent umbilical stump bleeding should be screened for factor XIII deficiency when routine coagulation tests prove normal.
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References
1.
Barbui T., Rodeghiero F., Dini E., et al. Subunits A and S inheritance in four families with congenital Factor XIII deficiency. Br J Haematol1978 ; 38:267-71.
2.
Duckert F., Jung E., Schmerling DHA hitherto undescribed congenital haemorrhagic diathesis probably due to fibrin stabilizing factor deficiency. Throb Diath Haemorrhagica1960;5:179-86.
3.
Kitchens CS, Newcomb TFFactor XIII. Medicine1979;58:413-29.
4.
Duckert F.Documentation of the plasma Factor XIII deficiency in man. Ann NY Acad Sci1972;202: 190-99.
5.
Francis J., Todd P.Factor XIII deficiency. Acta Haematol1979 ;62, 167-72.
6.
Francis J., Todd P.Congenital Factor XIII deficiency in a neonate. Br Med J1978;2:1532.
7.
Forman WB, Bayer R., Hadady M., Krill C., Lubin A.Congenital fibrin stabilizing factor deficiency (F.S.F. XIII): evidence for Dys F.S.F (abstract). Blood1977;50(Suppl. 1):266.