Medicine is that branch of science that helps us to know a human body and treat it in the right way to stay healthy as long as possible. So there are different factors which intrigue a person to chose medicine as their career of choice.
<h3><u>Explanation:</u></h3>
Medicine practically deals with knowledge about different disabilities as well as diseases that can attack a person to disturb his normal way of life. And for knowing the diseases, the medical practitioner needs to the normal functions of human body too. This fact attracts many person who are keen to know which mechanisms are going inside their body without even their knowledge.
Medicine also deals with different chemicals and compounds that are actually helpful in curing a disease. Thus, helping a person who is suffering from so much of pain because of a disease is so satisfying. There are many doctors who actually help different poor people who can't afford a good medical treatment. So medicine as a career is full of knowledge and experience, so worth taking as well.
Answer:
1) the genes and chromosomes do not double after each generations because parental sex cells are haploid and only contain one set of chromosomes. During fertilization the two cells fuse to form a diploid zygote with two copies of genes and chromosomes. For example a normal human has 46 chromosomes (2 copies of 23 chromosomes) during reproduction gametes which contain 23 chromosomes (haploid) fuse to form an offspring with the correct number of chromosomes ( 23 + 23 = 46).
2) offspring only receive one set of chromosomes from each parent so to maintain the chromosome number of humans. If this did not happen you would not be the same species.
1.) Achodroplasia is a autosomal dominant disorder, the suspected case suggested that inorder for the parents to produce and offspring with achondroplasia. One parents must have a single mutant gene of achodroplasia to be inherited by his offspring. for this case, It is suggested that the offspring might have developed its own mutant gene as it only affect 1 in 25,000 birth. There is changes of genes during early development.
2.) The mother said that they don't have that history of disorder. again, it's autosomal dominant disorder. one parents must have that kind of disorder so their child can also inherit it. Thus, no of the childs parents is a carrier.
It will help treat it, there's Hope of slowly treating it you have to have faith and patience.
Hope this helps :)
T-cells are a type of white blood cell that circulate around our bodies, scanning for cellular abnormalities and infections.
