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What else can I help you with?
What protein is missing or defective in hemophilia?
Hemophilia is a genetic disorder caused by a deficiency or defect in clotting factor VIII (hemophilia A) or factor IX (hemophilia B). These clotting factors are essential for blood clot formation, and their deficiency leads to prolonged bleeding and poor clotting ability.
Heamophilia is an example of what?
Hemophilia is an example of a genetic disorder that affects the body's ability to form blood clots, leading to excessive bleeding and bruising. It is caused by a deficiency in clotting factors, most commonly factor VIII or IX.
Is hemophilia a genetic disorder in which an abnormal form of hemoglobin is produced?
Hemophilia is not related to hemoglobin. It is a genetic disorder that affects the blood's ability to clot due to a deficiency in clotting factors. Hemoglobinopathies, on the other hand, are disorders related to the structure and production of hemoglobin.
Is vitamin K deficiency a cause of bleeding disorders?
Vitamin K is necessary for the production of Clotting Factors II, VII, IX and X. So a vitamin K deficiency could lead to a bleeding disorder. Additionally vitamin K is necessary for the production of the anticoagulant protein C and protein S. Inhibition of Vitamin K function is also associated with clotting disorders though for this to occur there has to be a deficiency in either proteins C or S.
What do all hemophilia suffers have in common?
All hemophilia sufferers have a deficiency in clotting factors, which are proteins needed to form blood clots and stop bleeding. This deficiency makes them prone to prolonged bleeding episodes even from minor injuries. Hemophilia is typically an inherited disorder caused by mutations in specific genes.
When APTT result low?
A low APTT result may suggest a bleeding disorder caused by factors like deficiencies in clotting factors (such as hemophilia) or the presence of inhibitors to clotting factors. Further evaluation is necessary to determine the specific cause of the prolonged APTT.
A hereditary bleeding disorder that results from lack of clotting factors?
Hemophilia is a hereditary bleeding disorder where a person lacks certain clotting factors, such as Factor VIII or Factor IX. This can result in prolonged bleeding and difficulty forming blood clots, leading to potential serious complications if not managed properly. Treatment often involves replacing the missing clotting factors through infusions.
What cell is infected with hemophilia?
Skin cells, I think. Hemophilia is when you can't heal outside wounds so I'm pretty sure it's skin. The person lacks certain protein for clotting factors. Platelets are used to clot the blood and make a person stop bleeding. Bleeding can occur internally as well as externally.
WhatSubstances that provide increased surface for platelet activation are known as?
clotting factors
What is hemopilia?
Hemophilia is a genetic blood disorder that affects the blood's ability to clot. This results in prolonged bleeding and difficulty stopping bleeding after an injury. There are different types of hemophilia, such as hemophilia A and hemophilia B, which are caused by deficiencies of specific clotting factors.
What is the organ that synthesizes most of the clotting factors?
Liver is responsible for the production of the clotting factors. Liver is the main organ of metabolism.
What is secondary enzyme deficiency caused from?
Secondary enzyme deficiency is caused by factors such as disease, medication, or surgery that disrupt normal enzyme function. These factors can lead to a reduction in the production or activity of enzymes, resulting in deficiency and impaired biochemical reactions in the body.
