Children are less likely to bring disease Hemophilia

Children are less likely to bring disease Hemophilia

Children are less likely to bring disease Hemophilia -- Hemophilia is a genetic disorder of the blood caused by a deficiency of blood clotting factors. Hemophilia A occurs if there is an abnormality in the gene that causes a lack of clotting factor VIII (FVII). Meanwhile, hemophilia B is caused lack of clotting factor IX (FIX). Hemophilia A and B can not be distinguished because they have a similar clinical appearance and a similar pattern of gene inheritance. The disease is not a contagious disease, but is for life or difficult to cure.

Physical abnormalities depending on the bleeding is going to be a hematoma in the head or extrinitis. and also frequently encountered hemartrasi. Of course there will be a feeling of hematoma area of pain. Rare gangrene. Interstial bleeding will cause muscle atrophy, movement would be disrupted, and sometimes causes peripheral neuritis.

There are two types of hemophilia:

- Type A or classic hemophilia, occurs due to deficiency of blood clotting factor VIII
- Type B occurs due to deficiency factors IX. These factors are proteins in the blood that cause problems in the process of blood clotting.

Hemophilia arguably occurred due to mutations in the gene that produces Factor VIII and IX. And, this gene mutation occurs on the X chromosome

Married men with hemophilia healthy women

Remember the basic principles of heredity. Females have a pair of sex chromosomes X and X. While men have X and Y chromosomes In conception, if he donates the X chromosome, which occurs offspring are girls. If he donated the Y chromosome, the offspring is happening is a boy.

That is, all the girls will be a carrier of hemophilia (a carrier), having inherited his father's X chromosome that carries the nature of hemophilia. And all the boys will not be exposed to hemophilia, because the Y chromosome inherited from the father.

Women married to men with hemophilia healthy

If they get a boy, the child has a chance of developing hemophilia by 50 percent. It depends on where the X chromosome in boys was obtained. If the boy was normal X chromosome inherited from the mother, so he will not have hemophilia properties. But, if he inherits the X chromosome carriers of hemophilia gene from the mother, then he will bring nature of hemophilia.

When they had a daughter, the possibility of bringing children with hemophilia trait is also 50 percent. Normal if the child will inherit a normal X chromosome from the mother. Instead, he can bring nature of hemophilia when inherited X chromosome that has hemophilia from mother nature.

Though the majority occur due to genetic factors, there are cases in which a child is born with hemophilia from parents and families healthy. This allows the event of a genetic mutation in the fetus.

Healing hemophilia disease

Hemophilia disease can be treated by eating jelly gamat Luxor, because:

1. Jelly Gamat Luxor contains EPA and DHA fatty acids which serves to repair damaged tissue.

2. Jelly Gamat Luxor is rich in collagen (80%), which plays a role in the blood clotting process.

3. Jelly Gamat Luxor contains a "cell growth factor" (cell growth factors) that will accelerate the formation of new tissue in the skin is scratched, cut, burned.