The possibility of child disease Hemophilia

Hemophilia is a genetic abnormality in the blood caused by lack of blood clotting factors. Hemophilia A occurs if there is an abnormality in the gene that causes a lack of clotting factor VIII (FVII). Whereas, hemophilia B is due to a lack of clotting factor IX (FIX). Hemophilia A and B cannot be distinguished because it has similar clinical appearance and similar gene inheritance pattern. The disease is not infectious diseases, but it is a lifetime or difficult to be cured.

Physical abnormalities depending on the bleeding is going on which can be either a hematom at the head or extrinitis. and also frequently encountered hemartrasi. Of course there will be a feeling of hematom area pain. Gangrene is rare. Interstial bleeding muscle atrophy will be menyebabk, the movement will be interrupted, and occasionally cause peripheral neuritis.

There are two types of Hemophilia:

-Type A or classic hemophilia, factor VIII deficiency occur due to blood clotting

-Type B occurs due to lack of factor IX. These factors are proteins in the blood that causes the problem in the process of blood clotting.

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

Men with hemophilia married women healthy

Remember the basic principles of offspring. Women have a pair of sex chromosomes, X and X chromosomes While men have. X and y. In conception, if men contributed to the X chromosome, of which occur are girls. If the man donated his Y chromosome, then the descent happened was a boy.

This means that all girls will be carriers of hemophilia (carrier), due to inherit the father's X chromosome which carries hemophilia properties. And all the boys will not be affected by hemophilia, because inherited Y chromosome from the father.

Women are hemophilia married men healthy

If they get the boy, the child has the possibility of getting hemophilia by 50 percent. It depends from which X chromosome in male children had. If the boy had inherited chromosome X is normal from the mother, so she will not have hemophilia. But, if she inherits an X chromosome gene carriers of hemophilia from the mother, then he will take the nature of hemophilia.

When they have girls, it is likely the child brings the nature of hemophilia is also 50 percent. Children will be normal if the normal X chromosome inherited from the mother. Instead, he could bring the nature of hemophilia if inherit the X chromosome that has the nature of hemophilia from the mother.

Although the majority occur due to genetic factors, there are cases where a child is born hemophilia from his parents and family healthy. "It is possible when there is a genetic mutation on the body of the fetus," said Chairman of the Indonesia Association of Hemophilia Society, Prof. Dr. Gatot Djajadiman, SpA (K), in the discussion welcomed the world hemophilia day on April 17.

Hemofili diseases can be treated by consuming jelly gamat Luxor, because:

1. Jelly gamat Luxor contains fatty acids EPA and DHA are working to repair damaged tissue.

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

3. Jelly gamat Luxor contains "cell growth factor" (cell grower factor) which will speed up the formation of new tissue on skin that is scratched, cut throat, burning.

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