| hemophilia |
Hemophilia is a genetic bleeding disorder that prevents blood from forming an effective clot. Without effective blood clotting, internal injuries and large external lacerations cannot heal properly. Hemophilia A and B are inherited as sex-linked recessive disorders occurring almost exclusively in males. Hemophilia has an estimated incidence of 1 in 5,000 males born in the United States and Canada. It is found in all ethnic groups in all parts of the world. ...
Ãâó: www.hemophiliagalaxy.com/general/encyclopedia.html
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| hemophilia |
a bleeding disorder in which a clotting factor (usually factor VIII or IX) is missing or does not function normally. Most people with hemophilia are male.
Ãâó: www.glhf.org/glossary.htm
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| hemophilia |
(Factor VIII, IX, X, XII) ?an inherited abnormality of the blood appearing only in the male population. The coagulation time of the blood is prolonged, despite the fact that bleeding time, prothrombin time, platelet count and tourniquet tests are normal. In the classical hemophilia (caused by a deficiency in Factor VIII) severe and prolonged hemorrhages can follow trivial injuries. This can pose a management problem during elective-type surgeries.
Ãâó: www.dentalinsurance.co.uk/implants/implant_glossar...
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| hemophilia A |
a bleeding disorder caused by deficiency in the activity of coagulation factor viii. affected individuals develop a variable phenotype of hemorrhage into joints, and muscles, easy bruising, and prolonged bleeding from wounds.
Ãâó: ipp.boku.ac.at/pz/ref/glossar1.html
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| hemophilia |
Term describing the condition in which patients have an abnormal tendency to bleed because they are unable to adequately form clots.
Ãâó: www-admin.med.uiuc.edu/hematology/Glossary.htm
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