Answer:
Decreased
Explanation:
Although there was a recent spike in the death rate of humans since 2019, the overall trend has been negative.
Source: The World Bank, which is a database that <em>"contains collections of time series data on a variety of topics"</em>
Answer:
An appropriate instruction for the parents would be to treat common flu with liquids
Explanation:
The medical support must examine the children's throat to determine if he need antibiotics, depending on the inspection they can decide the necessity of that kind of medicine.
Also the body temperature of the children is slightly high but not in a situation of alarm, his SpO2 is normal, there aren't any anomalies in his breath sounds, his pulse is normal for a 6 year old kid the parameters are from 75 to 115 beats per minute and he is 124 so is slightly elevated but not in terms to diagnose tachycardia. His breath frequency is in normal parameters for a 6 year old kid that should be from 15 to 20 breaths per minute.
So in conclusion there isn't any clinical situation that indicates a major medical problem with the pediatric patient. Treatment should be liquids to recover from the flu, antibiotics for laryngitis in case of needed with examination and antipyretic with analgesic aid such as ibuprofen.
Answer:
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Explanation:
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Garrod hypothesized that "inborn errors of metabolism" such as alkaptonuria occur because...genes dictate the production of specific enzymes, and affected individuals have genetic defects that cause them to lack certain enzymes.
Explanation:
Archibald Garrod researched on alkaptonuria and proposed the ‘one gene-one enzyme’ hypothesis. This led to the finding that alkaptonuria is caused due to an inherited or “inborn error of metabolism”.
This hypothesis stated that each gene codes and responsible for a single specific enzyme which facilitates a particular step in the metabolic processes.
According to Garrod, a mutation of a particular gene leads to specific error or defect leading to a lack of a particular enzyme that takes part in the biochemical metabolic pathways. This disrupts the metabolic pathway at the specific enzymatic action point.
In alkaptonuria, it was found that the defective phenotype of dark urine is due to the inborn error happening during the waste elimination process.
