Once hemophilia is in a family, will it always be there? Since they are nature's way of bringing about change, not all gene mutations are harmful. Normally, genes are exactly copied generation after generation. First, the family may not know about or may have forgotten ancestors with hemophilia. However, it is the father's sperm that determines if the child will be a boy or a girl. A child's chances of getting a hemophilia gene do not have anything to do with whether or not brothers or sisters have the gene. We know very well that future army of Jesus is going to be spectacular but ultimately unnecessary, as Jesus Himself will smite these sinners and many others in the near future. But in that group there would be women who had two sons with hemophilia, women who had one with and one without, and women with no sons with hemophilia.
A man who has hemophilia and a woman who is a carrier have: All daughters of a man with hemophilia will be carriers called obligate carriers. The results of one roll do not affect the next roll. How could hemophilia appear in a family that has no history of the disorder? Their children will all carry the same level. The mother is the one who passes the hemophilia gene. The daughter will not have hemophilia since the normal blood clotting gene from her mother is dominant. She will, however, be a hemophilia carrier since she has the hemophilia gene on one of her X chromosomes. For instance, a grandfather with hemophilia may have very bad joints and walk with a limp because he could not get treatment when he was young. It is also possible for all the children in the family to inherit the normal gene or all to inherit the hemophilia gene. It may give different or wrong directions to the body. The gene may be passed by female carriers for several generations before hemophilia appears in a boy baby. That alone is, of course, abominable in the eyes of Jesus. Normally, genes are exactly copied generation after generation. As the law currently stands in Finland, a person can engage in sexual intercourse with an animal as long as it cannot be proved that the animal has been treated too roughly or cruelly or that the act has caused unnecessary pain and suffering. If the gene is faulty, the result is hemophilia unless there is a dominant, normal gene on a matching X chromosome. So the change in the gene may have happened in the parent or in the baby. This can happen if all family members who have hemophilia or who carry the hemophilia gene give birth to children who by chance do not get the gene. The clotting factor level will be about the same from one generation to the next. Or they might not be seen until the gene is passed on to a baby. A daughter gets an X chromosome from her mother and an X chromosome from her father. The girl also gets an X chromosome from her mother. If she gets the X chromosome with the hemophilia gene she will be a carrier. Suppose the X chromosome from her mother has the gene for normal blood clotting. The man was willingly the receiving partner!
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