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Answer:
B)"My children who don't have the disease still run the risk of passing it on to their children.
Explanation:
Genetic diseases can be defined as alterations in the nucleotide sequence in a part of DNA that alter the structure of a protein and consequently cause anatomical and physiological abnormalities. These diseases are relatively rare, usually affecting few individuals in the population. These diseases can be defined into two main groups: those that affect only one gene and those that affect several. When only one gene changes, we say it is a monogenetic disease; When more than one gene has been affected, we say they are multifactorial diseases, also called polygenic.
Dominant autosomal disorders are mostly monegenic and are passed from parents to children through chromosomal inheritance. Thus, as children receive chromosomes from each of their parents, and chromosomes establish a relationship of dominance and recessivity among themselves, children may even inherit a gene that codes for an autosomal dominant disorder, however, these children may not develop this disorder if this gene responsible for it is on a recessive chromosome.
Determining why you eat certain foods is an example of analyzing influences.
Answer:
fasting plasma glucose test
Explanation:
The "fasting plasma glucose test" (FPG) is a diagnostic test being used to know whether people have diabetes,<em> a condition of having high levels of sugar in the blood</em>. This is being done by letting the patient fast for at least 8 hours. This will check the level of fasting blood sugar. If the level is greater than 126 mg/dL, then the person has a<em> positive result.</em> In order to confirm, another test will be done on the following day in the morning.
