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What is hemophilia commonly called?
Many years ago, it was refered to as 'the Royal Disease" also the "Bleeding disease". Hemophilia B is also known as Christmas Disease.
What is the nickname for hemophilia?
hemophilia B is also known as Christmas disease because Stephen Christmas was the first patient with the disease, and hemophilia A is just known as classic hemophilia.
Royal hemophilia is the result of inheritance?
Royal Hemophilia is a reference to Hemophilia B, also known as Factor IX (9) deficiency. This is a genetic disorder that can be inherited. Also near 30% of the Hemophilia B cases result from spontaneous mutations and are not inherited at all. That being said, once the mutation has occurred, that individual can pass the mutation on.
What is hemophilia A B or C?
First of all, there is no such thing as hemophilia C. Second, Type A: A mutation in the factor VIII gene. Type B: A mutation in the IX gene. Both of these genes are need to help clot the blood and close wounds(scabbing).
What gene or chromosome is mutated in the hemophilia disorder?
There are two types of hemophilia. Type A: A mutation in the factor VIII gene. Type B: A mutation in the IX gene.
Which is called Christmas disease in Christmas?
Hemophilia B is called Christmas disease after Stephen Christmas, the first patient suffering from it.
What is hemophilia commonly called?
Many years ago, it was refered to as 'the Royal Disease" also the "Bleeding disease". Hemophilia B is also known as Christmas Disease.
What is the nickname for hemophilia?
hemophilia B is also known as Christmas disease because Stephen Christmas was the first patient with the disease, and hemophilia A is just known as classic hemophilia.
What is Christmas disease also known as?
Hemophilia B.
What is the difference between Hemophilia A and Hemophilia B?
There are two types of hemophilia: hemophilia A (sometimes called classical hemophilia) and hemophilia B (sometimes called Christmas disease). Both are caused by a low level or absence of one of the proteins in the blood (called factors) that control bleeding. Hemophilia A is caused by a deficiency of factor VIII, and hemophilia B is caused by a deficiency of factor IX. There is no difference between the two types of hemophilia, except that hemophilia B is about five times less common than hemophilia A.
What is an inherited abnormality that causes a deficiency of a specific clotting factor resulting in a reduced ablitity to clot blood?
Hemophilia is a bleeding disorder that slows down the blood clotting process. People who have hemophilia often have longer bleeding after an injury or surgery. People who have severe hemophilia have spontaneous bleeding into the joints and muscles. Hemophilia occurs more commonly in males than in females.The two most common types of hemophilia are hemophilia A (also known as classic hemophilia) and hemophilia B (also known as Christmas disease). People who have hemophilia A have low levels of a blood clotting factor called factor eight (FVIII). People who have hemophilia B have low levels of factor nine (FIX).The two types of hemophilia are caused by permanent gene changes (mutations) in different genes.
Royal hemophilia is the result of what inheritance?
Hemophilia is broken into three subcategories; Hemophilia A, Hemophilia B, and Hemophilia C. These subcategories designate a person as having a deficiency of one of three specific clotting proteins. Hemophilia A is the deficiency of the protein called Clotting Factor VIII. Hemophilia B is the deficiency of Clotting Factor IX. Hemophilia C is the deficiency of Clotting Factor XI. "Royal" hemophilia is simply a reference to Hemophilia B and is therefore a result of a deficiency in the Clotting Factor IX protein. It is sometimes called the royal disease because it has been known to have been passed through some royal families throughout history.
What is the synonym of the leukemia?
it probay one of these, Christmas disease, Hand-Schuller-Christian disease, Letterer-Siwe syndrome, acute leukemia, anemia, angiohemophilia, aplastic anemia, chronic leukemia, cyclic neutropenia, erythrocytosis, hemoglobinopathy, hemophilia, hemophilia A, hemophilia B, hypochromic anemia, infectious granuloma, iron deficiency anemia, leukemic reticuloendotheliosis, macrocytic anemia, multiple myeloma, myelogenous leukemia, neutropenia, pernicious anemia, plasma cell leukemia, plasmacytoma, polycythemia, pseudoleukemia, purpura, purpura hemorrhagica, sickle-cell anemia, thalassemia, vascular hemophilia glad to help!
Royal hemophilia is the result of inheritance?
Royal Hemophilia is a reference to Hemophilia B, also known as Factor IX (9) deficiency. This is a genetic disorder that can be inherited. Also near 30% of the Hemophilia B cases result from spontaneous mutations and are not inherited at all. That being said, once the mutation has occurred, that individual can pass the mutation on.
What is the cure for hemophilia b?
Other than a liver transplant the is hardly an ideal solution, there is no cure for Hemophilia A or B as of yet.
Did Mother Teresa have hemophilia?
She is rumored to have Hemophilia type B. no one is sure if it is true.
What happens if hemophilia b gets diagnosed as hemophilia a?
it will become more superstitious or it will become powerful.
