haemophilia

الإنجليزية - التركية

تعريف haemophilia في الإنجليزية التركية القاموس.: hemofili; {i} kan hastalığı; (Diş Hekimliği) kadınların taşıyıcı olduğu ve sadece erkeklerde görülen ırsi kan pıhtılaşma bozukluğu
hemophilia: (Tıp) hemofili hastalığı
hemophilia: (Tıp) Pıhtılaşma yeteneğinin yokluğu, yalnız erkeklerde görülen kanama istidadı, hemoflii
hemophilia: hemofili kanın pıhtılaşmaması
hemophilia: {i} kan hastalığı
hemophilia: {i} hemofili
Tom bir hemofili hastası. - Tom is a hemophiliac.
hemophilia: i., tıb. hemofili

الإنجليزية - الإنجليزية

تعريف haemophilia في الإنجليزية الإنجليزية القاموس.: Any of several hereditary illnesses that impair the body's ability to control bleeding, usually passed from mother to son; haemo·philia in AM, use hemophilia Haemophilia is a medical condition in which a person's blood does not thicken or clot properly when they are injured, so they continue bleeding. hemophilia a serious disease that prevents a person's blood from becoming thick, so that they lose a lot of blood easily if they are injured; an inherited blood disorder which results in the blood not clotting properly; congenital tendency to uncontrolled bleeding; usually affects males and is transmitted from mother to son; Any of several hereditary illnesses that impair the bodys ability to control bleeding, usually passed from mother to son; {i} hereditary disorder characterized by a failure of the blood to clot normally; A hereditary blood disease where the blood fails to clot and abnormal bleeding occurs It is only found in males and is treated by injections of Factor VIII - a blood product used to assist clotting function; A rare, hereditary bleeding disorder caused by a deficiency in the ability to synthesize one or more of the coagulation proteins; e g Factor VIII (Haemophilia A) or Factor IX (Haemophilia B)
hemophilia: disease in which the blood does not clot properly after an injury The result can be serious internal bleeding It is suffered mainly by males, who inherit it from their mothers
hemophilia: A largely inherited clotting disorder that occurs almost exclusively in males The disorder delays coagulation, making bleeding difficult to control
hemophilia: any of several hereditary blood-coagulation disorders in which the blood fails to clot normally because of a deficiency or an abnormality of one of the clotting factors; hemophilia, a recessive trait associated with the X-chromosome, is manifested almost exclusively in males
hemophilia: congenital tendency to uncontrolled bleeding; usually affects males and is transmitted from mother to son
hemophilia: An inherited disease that affects mostly males and prevents normal blood clotting It is treated by lifelong injections of a synthetic version of the clotting factor lacking in persons with the disease
hemophilia: {i} hereditary disorder characterized by a failure of the blood to clot normally
hemophilia: Term describing the condition in which patients have an abnormal tendency to bleed because they are unable to adequately form clots
hemophilia: an inherited bleeding disorder caused by low levels, or absence of, a blood protein that is essential for clotting; hemophilia A is caused by a lack of the blood clotting protein factor VIII; hemophilia B is caused by a deficiency of factor IX
hemophilia: see haemophilia. the American spelling of haemophilia (hemo- + -philia). Hereditary bleeding disorder caused by deficiency of a coagulation factor. Lack of factor VIII causes classic hemophilia; other types are caused by deficiency of factor IX or XI. The first two are transmitted by sex-linked heredity; the third has dominant inheritance and occurs in females as well as males. Spontaneous bleeding may occur. Even trivial injury can cause life-threatening blood loss. Drugs can be given to stop bleeding. Heavy blood loss requires blood transfusions
hemophilia: An inherited deficiency in blood-clotting ability, which can cause serious internal bleeding
hemophilia: familial disease appearing in males, transmitted by females, characterized by absence of specific globulin in blood and imperfect coagulation
hemophilia: An inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhages spontaneous or traumatic, because of the result of a missing or a low amount of one of the clotting factors
hemophilia: An X-linked recessive genetic disease, caused by a mutation in the gene for clotting factor VIII (hemophilia A) or clotting factor IX (hemophilia B), which leads to abnormal blood clotting