Stroke, Vol 21, 1077-1080, Copyright © 1990 by American Heart Association
J Kohler, J Kasper, I Witt and GM von Reutern
Plasma protein C exerts anticoagulatory effects by inactivating factors V
and VIII. Hereditary protein C deficiency is transmitted as an autosomal
dominant disorder. Homozygous individuals usually develop purpura fulminans
as newborns; heterozygous protein C-deficient individuals are at increased
risk for venous thrombosis and pulmonary embolism. However, arterial
thrombosis has been only rarely observed. We describe a young patient with
heterozygous protein C deficiency who experienced a severe stroke due to
thrombotic occlusion of the left middle cerebral artery.
ARTICLES
Ischemic stroke due to protein C deficiency
Department of Neurology, University of Freiburg, Federal Republic of Germany.
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