The
lack of the enzyme glucose -6 - phosphate Diedroginas (G6PD) in red
blood cells, which was discovered in 1956, one of the most common
genetic diseases, if you are suffering more than 400 million people all
over the world of this shortfall. Called
the lack of this enzyme, anemia beans favism because individuals
infected with the shortage of people with allergy to plant beans. People
with a lack of activity of this enzyme are at risk for a number of
serious disorders which can lead to death if not treated properly.
In short, the beans favism anemia is a severe hemolytic anemia, usually occurs in people descended from the Mediterranean region, and occurs when a person with a lack of the enzyme glucose -6 - phosphate Diedroginas eating beans or inhale pollen beans.
G6PD enzyme deficiency in the science of geneticsIt is known that in humans there are 23 pairs of chromosomes that determine the meta-physical qualities and metabolic variety. One of these pairs of 23 chromosomes is a pair of X and Y chromosome X and Y (known Pkromusumaat sex) that determine the sex of the individual as well as other things. X chromosome is particularly important because it carries the genes essential for human survival. There is an important gene in chromosome X, Hu enzyme G6PD.
All genetic diseases related to the X chromosome, such as lack of the enzyme G6PD, affecting males more than females. G6PD deficiency will appear in females only when there are two copies of the gene Maeptan in the female. As long as I found one copy is valid for G6PD gene in a female, it will produce a natural enzyme and this enzyme can act as a natural enzyme defective. When you receive the advantage of a specific culture in such a manner known as recessive genetic recipe. In males, and because of the presence of X chromosome and only one, emergence of G6PD gene defective one be enough for a lack of the enzyme G6PD.
It is known that there are more than 400 strain or a different form for the same gene that causes a lack of the enzyme G6PD. G6PD defective enzyme may be different from person to person. Gene mutations differ from one region to the other, but residents of a particular area usually share those boom. For example, in Egypt exists only one type of strain is called "strain or mutation of the Mediterranean" Mediterranean variant, while in Japan there is a different type of mutation called Japan Japan variant.
What are the chances of inherited enzyme deficiency to their children?
If the father was injured and the mother is not infected and not carrying the gene
The proportion of female to have infected (zero%)
The proportion of infected male births (zero%)
The proportion of female to have the holder of a lack of the enzyme gene G6PD (do not show any symptoms) (100%)
If the father was injured and the mother is a carrier of the gene
The proportion of infected female births (50%)
Having a pregnant female ratio of the gene (50%)
The proportion of infected male births (50%)
If the father is injured and the mother is a carrier of the gene
The proportion of female to have infected (zero%)
Female reproductive rate, carrying the gene (50%)
The proportion of infected male births (50%)
In short, the beans favism anemia is a severe hemolytic anemia, usually occurs in people descended from the Mediterranean region, and occurs when a person with a lack of the enzyme glucose -6 - phosphate Diedroginas eating beans or inhale pollen beans.
G6PD enzyme deficiency in the science of geneticsIt is known that in humans there are 23 pairs of chromosomes that determine the meta-physical qualities and metabolic variety. One of these pairs of 23 chromosomes is a pair of X and Y chromosome X and Y (known Pkromusumaat sex) that determine the sex of the individual as well as other things. X chromosome is particularly important because it carries the genes essential for human survival. There is an important gene in chromosome X, Hu enzyme G6PD.
All genetic diseases related to the X chromosome, such as lack of the enzyme G6PD, affecting males more than females. G6PD deficiency will appear in females only when there are two copies of the gene Maeptan in the female. As long as I found one copy is valid for G6PD gene in a female, it will produce a natural enzyme and this enzyme can act as a natural enzyme defective. When you receive the advantage of a specific culture in such a manner known as recessive genetic recipe. In males, and because of the presence of X chromosome and only one, emergence of G6PD gene defective one be enough for a lack of the enzyme G6PD.
It is known that there are more than 400 strain or a different form for the same gene that causes a lack of the enzyme G6PD. G6PD defective enzyme may be different from person to person. Gene mutations differ from one region to the other, but residents of a particular area usually share those boom. For example, in Egypt exists only one type of strain is called "strain or mutation of the Mediterranean" Mediterranean variant, while in Japan there is a different type of mutation called Japan Japan variant.
What are the chances of inherited enzyme deficiency to their children?
If the father was injured and the mother is not infected and not carrying the gene
The proportion of female to have infected (zero%)
The proportion of infected male births (zero%)
The proportion of female to have the holder of a lack of the enzyme gene G6PD (do not show any symptoms) (100%)
If the father was injured and the mother is a carrier of the gene
The proportion of infected female births (50%)
Having a pregnant female ratio of the gene (50%)
The proportion of infected male births (50%)
If the father is injured and the mother is a carrier of the gene
The proportion of female to have infected (zero%)
Female reproductive rate, carrying the gene (50%)
The proportion of infected male births (50%)
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