Because of symptoms and age, we would consider some diagnosis of bronchitis due to RSV infection, pneumonia because of Haemophilus influenza infections, and pertussis infection including apnea. Here I can say the answer is pneumonia due to infection of Haemophilus influenza.
The kind of treatment we can give depending on my diagnosis are; high dosage of oral erythromycin to clear the infection bacteria, supportive therapies in hospital in order to maintain blood oxygen levels and in open airways, low dosage of erythromycin which is given intravenously to clear the infection of bacteria which I can say it is the best treatment.
Some of the treatment for the infant to diminish such infection chances are MMR vaccines, toxin antiserum DTaP vaccine, influenza shot which I can recommend for the infant.
The best reason I can say about these conditions and symptoms are associated with pneumonia whereby we can say the low dose of erythromycin which is given intravenously is effective. The best prophylactic treatment is influenza shots.
Chlorophyll is a green pigment found in plants. Plants use chlorophyll and light to make food.
Answer:
1500
Explanation:
Let's assume that the allele for yellow seed color is "Y" and the allele for green seed color is "y". Genotype of pure breeding yellow seeded plant would be "YY" and that of the green seeded plant would be "yy". A cross between YY and yy gives all heterozygous yellow seeded plants (Yy) in F1 progeny. Self pollination of two F1 plants (Yy x Yy) obtains F2 generation in 3 yellow: 1 green ratio.
The total population size of F2 generation = 2000
The proportion of yellow seeded plants in F2 generation = 3/4 (since the F2 phenotype ratio is given 3 yellow: 1 green)
Therefore, total number of yellow seeded plants in F2 progeny = 3/4 x 2000= 1500
Answer:
* Infectious disease management depends on precise portrayal of disease progression so transmission can be forestalled. Gradually progressing infectious diseases can be hard to characterize because of a latency period between the time an individual is infected and when they show clinical signs of disease.
* Defining directions through sickness states from infection to clinical illness can assist researchers with creating control programs dependent on focusing on individual infection state, possibly decreasing both progression and creating misfortunes because of the illness.
Explanation:
Gradually progressing infectious diseases are hard to characterize in light of the fact that they are frequently connected with an inactivity period between the time an individual is infected and when they give clinical indications or side effects of illness.
To successfully control infectious diseases, it is paramount to see how the disease progresses.
Answer: Read explanation
Explanation: there’s actually no similarity at all. A cell membrane is made of phospholipids, globular proteins, glycolipids, glycoproteins, and cholesterol, and has passages that serve explicitly for passive and active transport of materials through it.
The skin is made of cells and dead keratin and serves as much as possible to prevent most substances from moving through it. It’s “designed” for toughness and distensibility, not for selective permeability.
All in all, the difference is that a cell membrane is explicitly and only for the passing and transport of materials through it, and the skin in the skin is made to be tough and durable, almost the opposite of a cell membrane.
