hemophilia

listen to the pronunciation of hemophilia
English - Turkish
hemofili

Tom bir hemofili hastası. - Tom is a hemophiliac.

(Tıp) Pıhtılaşma yeteneğinin yokluğu, yalnız erkeklerde görülen kanama istidadı, hemoflii
hemofili kanın pıhtılaşmaması
{i} kan hastalığı
i., tıb. hemofili
(Tıp) hemofili hastalığı
hemophilia b
hemofili b
haemophilia
{i} kan hastalığı
haemophilia
(Diş Hekimliği) kadınların taşıyıcı olduğu ve sadece erkeklerde görülen ırsi kan pıhtılaşma bozukluğu
haemophilia
{i} hemofili
English - English
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
A largely inherited clotting disorder that occurs almost exclusively in males The disorder delays coagulation, making bleeding difficult to control
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
congenital tendency to uncontrolled bleeding; usually affects males and is transmitted from mother to son
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
{i} hereditary disorder characterized by a failure of the blood to clot normally
Term describing the condition in which patients have an abnormal tendency to bleed because they are unable to adequately form clots
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
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
An inherited deficiency in blood-clotting ability, which can cause serious internal bleeding
familial disease appearing in males, transmitted by females, characterized by absence of specific globulin in blood and imperfect coagulation
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
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
Hemophilia B
{i} (Haematology) Hemophilia B, hereditary blood coagulation disorder, form of haemophilia caused by congenital deficiency of clotting factor IX in the blood
hemophilia a
hemophilia caused by a congenital deficiency of factor VIII; occurs almost exclusively in men
hemophilia a
a condition caused by a lower-than-normal amount of factor VIII
hemophilia a
A bleeding disorder that stems from a deficiency or abnormality of factor VIII, which impairs the body’s ability to form fibrin clots during the clotting process Sometimes called classic or standard hemophilia
hemophilia a
a blood clotting disorder caused by a gene on the X chromosome
hemophilia b
a clotting disorder similar to hemophilia A but caused by a congenital deficiency of factor IX
haemophilia
Any of several hereditary illnesses that impair the body's ability to control bleeding, usually passed from mother to son
haemophilia
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
haemophilia
an inherited blood disorder which results in the blood not clotting properly
haemophilia
congenital tendency to uncontrolled bleeding; usually affects males and is transmitted from mother to son
haemophilia
Any of several hereditary illnesses that impair the bodys ability to control bleeding, usually passed from mother to son
haemophilia
{i} hereditary disorder characterized by a failure of the blood to clot normally
haemophilia
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
haemophilia
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

    Hyphenation

    he·mo·phi·li·a

    Turkish pronunciation

    himıfiliı

    Pronunciation

    /ˌhēməˈfēlēə/ /ˌhiːməˈfiːliːə/
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