What type of mutation is hemophilia, deletion, insertion, duplication, translocation, or inversion?
She is rumored to have Hemophilia type B. no one is sure if it is true.
There is no single type of mutation that causes Hemophilia A. It is not the type of mutation but rather the location of the mutation within the genetic code.
No specific type of mutation
X-linked recessive is the type of inheritance pattern that hemophilia and color blindness show.
Hemophilia type A is when your blood is missing Factor VIII (8) of the 13 clotting factor proteins involved in the clotting process. In type B, the blood is missing Factor IX (9).
There are two types of hemophilia. Type A: A mutation in the factor VIII gene. Type B: A mutation in the IX gene.
It is named after the first patient who was described with the symptoms of Hemophilia type B, Stephen Christmas.
People with hemophilia are born with it. Hemophilia is a hereditary disease - in other words, it "runs in families" (is inherited). There is another type of hemophilia called acquired hemophilia. Acquired hemophilia results from the development of autoantibodies (mostly of the IgG1 and IgG4 subclasses) directed against clotting factors. Acquired hemophilia can be brought on by reactions to medications such as penicillin, sulfonamides, phenytoin, methyldopa, chloramphenicol, interferon alpha, and others.
just type in history of hemophilia on google, click on the first hit, and its all there. :) hope i helped....btw its kinda a weird history just type in history of hemophilia on google, click on the first hit, and its all there. :) hope i helped....btw its kinda a weird history
That depends on the type of hemophilia. There is a condition called Acquired Hemophilia that is not genetic and therefore not inheritable. Traditional hemophilia is genetic and therefore is inheritable. Due to the nature of the disorder, traditional hemophilia can be cause by random mutations at the time of birth as well, meaning that the individual can have genetic hemophilia without actually inheriting it from their parents. Once this mutation has occurred, the individual can pass the trait on to their children and future generations.
The probability that their son has hemophilia is 50%.
In the most common type, Hemophilia A, the person lacks clotting factor VIII. In Hemophilia B, clotting factor IX is lacking.
XhXh - with hemophilia XhXH- carrier of hemophilia
Hemophilia is not contagious.
Yes - there are dogs with hemophilia. German Shepards in Europe with hemophilia can be traced back to one dog: Canto von der Wienerau. For more informationon hemophilia and dogs: http://mydogfluffy.com/faq.htm Mice with hemophilia are used to research hemophilia medication and a cure for hemophilia.
Both Hemophilia A and Hemophilia B are X-Linked Recessive.
It depends on the type and severity of the hemophilia. There are many types, and some of the less severe types, a gentle massage may be applied with a doctor's clearance.
Hemophilia is an X-lined recessive disease. It is caused by a mutation of the F8 gene as in hemophilia A, and F9 gene as in hemophilia B.
Hemophilia A is the most common form of Hemophilia. Approximately, 1 in 5,000 males are affected by Hemophilia A.
Hemophilia A - Factor VIII Hemophilia B - Factor IX Hemophilia C - Factor XI
Hemophilia is blood that does not clot.
Color Blind is a Sex-Linked characteristic.
Yes, hemophilia is an autosomal recessive disorder. Hemophilia A and hemophilia B are inherited in an X-linked recessive pattern.