Answer:
This could be possible if the wife is a carrier of the FMO3 allele. Therefore the two carrier parents must have passed the defective alleles to the child, who now possessed the gene for the FMO3, and said to be dominant for the fish odor.
In genetics a Carrier is an individual who inherited a defective allele (FMO3) , but do not show the manifestations of the allele, or symptoms of the diseases attributed to it. Therefore the wife is a Carrier for the allele if the child could show this symptoms of fish odor.
Explanation:
The presentation of an 18-month-old with hereditary fructose intolerance (HFI), deficiency of aldolase B and low blood glucose levels is due to accumulation of fructose-1 phosphate and the inhibition of glycolytic-gluconeogenic pathways.
Explanation:
Hereditary fructose intolerance leads to deficiency of fructose-1-phosphate aldolase enzyme. This enzyme deficiency leads to accumulation of fructose-1 phosphate in the liver. Fructose-1 phosphate inhibits the action of phosphorylase enzyme which monitors the glycogen to glucose conversion. Since glucose formation is reduced, hypoglycemia and lactic acidosis takes place accounting for the patient’s low blood sugar.
Decomposer- <span>an organism, especially a soil bacterium, fungus, or invertebrate, that decomposes organic material.</span>
Scientist rely on <em>Biology </em>concepts when researching crop production and medicine.
The inference would be that the Rock and roll band member lost some of his/her hearing from loud music.