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A blood coagulation disorder due
to factor XII deficiency. Factor XII is a plasma protein which on activation by
surface contact sets off chain reactions activating the clotting of blood,
kinin, fibrinolytic and complement pathways. In a deficiency of Hagemann’s factor
there is a sustained coagulation time, but rarely haemorrhagic symptoms. Asymptomatic
with few minor exceptions. Laboratory curiosity. Inheritance is autosomal
recessive. Families with autosomal dominant condition found.
Bibliography
Oscar D. Ratnoff and Joan E. Colopy:
• A familial hemorrhagic trait associated with a deficiency of a clot-promoting
fraction of plasma.
Journal of clinical investigation, New York, 1955; 3: 602-613.
Oscar D. Ratnoff, R. J. Busse and R. P. Sheon:
• The demise of John Hageman.
New England Journal of Medicine, Boston, 1979: 260-261.
• A familial hemorrhagic trait associated with a deficiency of a clot-promoting
fraction of plasma.
Journal of clinical investigation, New York, 1955; 3: 602-613.
Oscar D. Ratnoff, R. J. Busse and R. P. Sheon:
• The demise of John Hageman.
New England Journal of Medicine, Boston, 1979: 260-261.