Causes, incidence, and risk factors: Congenital protein C or S deficiency is an inherited disorder that causes abnormal blood clotting. Normal blood coagulation is a complex process involving as many as 20 different plasma proteins known as coagulation factors.
A series of complex chemical reactions using these factors takes place very rapidly to form an insoluble protein called fibrin, which stops bleeding. Other plasma proteins, such as proteins C and S, inhibit or reverse this process to prevent excessive clotting.
When certain coagulation factors are deficient or missing, the chain reaction does not take place normally. In this disorder, an increased risk of clot formation, called thrombosis, is present. Risk factors are an individual or family history of recurrent blood clots in the veins.
There are different types of genetic transmission of this disease. Heterozygous (one normal gene and one defective) protein C deficiency occurs in approximately 1 in 300 members of the general population. Protein S deficiency occurs in about 1 in 20,000 people.
Prevention: If the disorder is diagnosed, precautions may be taken to avoid thrombus formation in high-risk situations that promote slow movement of the blood in the veins. This occurs with prolonged bed rest usually as a result of an illness, surgery, or hospitalization.