Severe factor V deficiency with prolonged bleeding time. 1974

K Breederveld, and E A van Royen, and J W Ten Cate

UI MeSH Term Description Entries
D001780 Blood Coagulation Tests Laboratory tests for evaluating the individual's clotting mechanism. Coagulation Tests, Blood,Tests, Blood Coagulation,Blood Coagulation Test,Coagulation Test, Blood,Test, Blood Coagulation
D001792 Blood Platelets Non-nucleated disk-shaped cells formed in the megakaryocyte and found in the blood of all mammals. They are mainly involved in blood coagulation. Platelets,Thrombocytes,Blood Platelet,Platelet,Platelet, Blood,Platelets, Blood,Thrombocyte
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D005166 Factor V Deficiency A deficiency of blood coagulation factor V (known as proaccelerin or accelerator globulin or labile factor) leading to a rare hemorrhagic tendency known as Owren's disease or parahemophilia. It varies greatly in severity. Factor V deficiency is an autosomal recessive trait. (Dorland, 27th ed) Owren Disease,Parahemophilia,Deficiency, Factor 5,Deficiency, Factor Five,Deficiency, Factor V,Factor 5 Deficiency,Factor Five Deficiency,Labile Factor Deficiency,Owren Parahemophilia,Owren's Disease,Deficiencies, Factor 5,Deficiencies, Factor Five,Deficiencies, Factor V,Deficiencies, Labile Factor,Deficiency, Labile Factor,Disease, Owren,Disease, Owren's,Factor 5 Deficiencies,Factor Five Deficiencies,Factor V Deficiencies,Labile Factor Deficiencies,Owrens Disease,Parahemophilia, Owren,Parahemophilias
D005260 Female Females
D006474 Hemorrhagic Disorders Spontaneous or near spontaneous bleeding caused by a defect in clotting mechanisms (BLOOD COAGULATION DISORDERS) or another abnormality causing a structural flaw in the blood vessels (HEMOSTATIC DISORDERS). Hemorrhagic Diathesis,Diatheses, Hemorrhagic,Diathesis, Hemorrhagic,Disorder, Hemorrhagic,Disorders, Hemorrhagic,Hemorrhagic Diatheses,Hemorrhagic Disorder
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D001017 Aortic Coarctation A birth defect characterized by the narrowing of the AORTA that can be of varying degree and at any point from the transverse arch to the iliac bifurcation. Aortic coarctation causes arterial HYPERTENSION before the point of narrowing and arterial HYPOTENSION beyond the narrowed portion. Coarctation of Aorta,Coarctation of Aorta Dominant,Coarctation of the Aorta,Aorta Coarctation,Aorta Coarctations,Aorta Dominant Coarctation,Aorta Dominant Coarctations,Aortic Coarctations,Coarctation, Aortic,Coarctations, Aortic

Related Publications

K Breederveld, and E A van Royen, and J W Ten Cate
August 1966, The New England journal of medicine,
K Breederveld, and E A van Royen, and J W Ten Cate
July 2014, Vox sanguinis,
K Breederveld, and E A van Royen, and J W Ten Cate
January 1971, Acta haematologica Polonica,
K Breederveld, and E A van Royen, and J W Ten Cate
November 1984, Lakartidningen,
K Breederveld, and E A van Royen, and J W Ten Cate
September 1972, Acta medica Scandinavica,
K Breederveld, and E A van Royen, and J W Ten Cate
September 2002, Turkish journal of haematology : official journal of Turkish Society of Haematology,
K Breederveld, and E A van Royen, and J W Ten Cate
May 1977, Blood,
K Breederveld, and E A van Royen, and J W Ten Cate
June 1973, The Journal of the Association of Physicians of India,
K Breederveld, and E A van Royen, and J W Ten Cate
December 1960, Harefuah,
K Breederveld, and E A van Royen, and J W Ten Cate
April 1986, Presse medicale (Paris, France : 1983),
Copied contents to your clipboard!