Medical Definition of Thrombotic disease due to protein c deficiency

1. Protein C is a protein in plasma that enters into the cascade of biochemical events leading to the formation of a clot. Deficiency of protein c results in thrombotic (clotting) disease and excess platelets with recurrent thrombophlebitis (inflammation of the vein that occurs when a clot forms). The clot can break loose and travel through the blood stream (thromboembolism) to the lungs causing a pulmonary embolism, brain causing a stroke (cerebrovascular accident), heart causing an early heart attack, skin causing what in the newborn is called neonatal purpura fulminans, the adrenal gland causing haemorrhage with abdominal pain, abnormally low blood pressure (hypotension), and salt loss. Protein c deficiency is due to possession of one gene (heterozygosity) in chromosome band 2q13-14. The possession of two such genes (homozygosity) is usually lethal. (12 Dec 1998)

Lexicographical Neighbors of Thrombotic Disease Due To Protein C Deficiency

thrombopoietins
thromboprophylaxis
thromboregulation
thrombose
thrombosed
thromboses
thrombosin
thrombosing
thrombosis
thrombospondin
thrombospondin 1
thrombospondins
thrombostasis
thrombosthenin
thrombotic
thrombotic disease due to protein c deficiency (current term)
thrombotic gangrene
thrombotic hydrocephalus
thrombotic infarct
thrombotic microangiopathy
thrombotic phlegmasia
thrombotic thrombocytopenic purpura
thrombotically
thrombotonin
thromboxane
thromboxane-a synthase
thromboxane a2
thromboxane b2
thromboxane dehydrogenase
thromboxanes

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