Answer: <em>D. Causes an accumulation of lipids in brain cells</em>
Explanation:
Tay-Sachs disease is caused by a genetic mutation in the <em>HEXA</em> gene. It is an autosomal recessive disease that causes the mutation on an enzyme, which metabolizes <em>GM2 Ganglioside</em> in nerve cells, this leads to a build-up of the molecule in brain cells. At the moment there is no cure for the disease, only support treatment is available.
The question offers an image containing information regarding the patient by the name of Anita and her actions prior to arriving at the hospital.
We can describe the patient and her timeline up to her hospital visit by mentioning information about her:
- <em>Name </em>
- <em>Occupation</em>
- <em>Weight</em>
- <em>Age</em>
- <em>Actions prior to her hospital visit</em>
The patient in question is a 108 pound, 36-year-old female by the name of Anita Martin. The patient is indicated to be a security guard. As per the information given, the patient seems to have been working a night shift in a building in the vicinity of a recent train wreck that seems to have released chlorine gas. On her way to her car, Anita was exposed to chlorine gas, due to which she decided to drive to the hospital.
With this information, we will have properly described the patient in question so that the medical professionals at the hospital will have all the information necessary to proceed with an effective treatment plan for Anita's condition.
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Blood typing can identify if will is the father or not by the composition of the genotype and it’s compatibility within the parents.
Will can not be the parent as there is only one possible genotype composition of blood type AB being i^Ai^B.
Idk exactly what you mean but I guess you can ask what kind of cell it has idk?
