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Protein S deficiency: A genetic condition where a person faces an increased risk of blood clot formation. It is characterized by a deficiency of functioning protein S which is a protein needed to regulate the blood clotting process. The homozygous form of the condition carries a much higher risk of thrombosis with severe thrombosis often occurring at birth. More detailed information about the symptoms, causes, and treatments of Protein S deficiency is available below.
Read more about symptoms of Protein S deficiency
Review possible medical complications related to Protein S deficiency:
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Read more about Misdiagnosis and Protein S deficiency
Medical research articles related to Protein S deficiency include:
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Visit our research pages for current research about Protein S deficiency treatments.
Read about other experiences, ask a question about Protein S deficiency, or answer someone else's question, on our message boards:
An autosomal dominant disorder showing decreased levels of plasma protein S antigen or activity, associated with venous thrombosis and pulmonary embolism. PROTEIN S is a vitamin K-dependent plasma protein that inhibits blood clotting by serving as a cofactor for activated PROTEIN C (also a vitamin K-dependent protein), and the clinical manifestations of its deficiency are virtually identical to those of protein C deficiency. Treatment with heparin for acute thrombotic processes is usually followed by maintenance administration of coumarin drugs for the prevention of recurrent thrombosis. (From Harrison's Principles of Internal Medicine, 12th ed, p1511; Wintrobe's Clinical Hematology, 9th ed, p1523) - (Source - Diseases Database)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Protein S deficiency as a "rare disease".
Source - Orphanet
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