Genetic factors of disease

Genetic factors of disease:-

By combining spermatozoa and ovum in the fallopain tube of the uterus, it first creates a zygote. and later it gradually collapses into a full human child. Now this spermatozoa and ovum have 23 pair of chromosome in each of the nuclei.These chromosomes are always the same in women ovum, they are called chromosome, but men have different types of spermatozoa - they are X and Y chromosomes.Now if X-chromosomes with ovum are mixed with worm, then X + X matches the female child and Y chromosomal with insect ovum, X + Y matches with son.

Now the 22 pairs of these 23 pairs of chromosomes look similar. But without it there is a pair of different types called sex chromosome.These are XX or XY chromosomes. There is always a sex chromosomal XX for women, it can be  XX or XY for men.

The object that enters the father and mother's child, is a substance called chromosomes, called DNA or Deoxyribonucleic acid. In this case, the tendency of disease or disease to be transmitted from the parents of the children. Again, many diseases can not be accumulated in this way. So the genetic factor is always helpful in determining the diagnosis of disease or the likelihood of disease to every doctor.

According to the symptoms, other treatments need to be done.

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