hemophilia
hemophilia
Hemophilia
Hemophilla is a genetic disorder in which there is absence of clotting factor viii, leading to defective clot formation, petechiae bruising and gum bleeding. Treatment is by injecting factor VIII concentrate
Hemophilia is a genetic blood clotting disorder.
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.
genetic disorder
Hemophilia
That is the definition of a genetic disorder.
The disorder that causes poor blood clotting is hemophilia. Hemophilia is a genetic disorder where the blood lacks certain proteins that help with clotting, leading to excessive bleeding and difficulty forming blood clots.
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.
False; Hemophilia is caused by a mutated allele that produces a defective form of the protein fibrin.Sickle Cell Disease is caused by a defective form of hemoglobin.
Color blindness is a sex-linked genetic disorder. The reason that it is more prevalent in males is because the disorder is linked the the X-chromasome. If a male inherits an X chromosome that is defective, then they will be color blind. However, a female has two X chromosomes which means she can receive a defective chromosome and only be a carrier of the mutation. If she receives two defective x chromosomes, she will be colorblind.