Answer:
There is no cure for cystic fibrosis, but treatment can ease symptoms and reduce complications.
Explanation:
1). For those with cystic fibrosis who have certain gene mutations, doctors may recommend a newer medication called ivacaftor. This medication may improve lung function and weight, increases the activity of Cystic fibrosis transmembrane conductance regulator (CFTR)protein and reduce the amount of salt in sweat. It has been approved by the Food and Drug Administration for people with cystic fibrosis who are age 6 and older. The dose depends on your weight and age.
2). For people with a certain gene mutation who are age 12 and older, another drug is available that combines ivacaftor with a medication called lumacaftor. This drug is called orkambi.
The use of Orkambi may improve lung function and reduce the risk of exacerbations.
I hope you're clear on this Daxxy
With what do you need help in, like the subject to indentify
most common to least common favorite
Answer: 0.18
Explanation:
For the alleles, the percentage distribution of each is 'A' (90% = 0.9)
While 'a' (10% = 0.1)
Hence, 0.9 and 0.1 are the respective frequencies of each allele
Now, apply Hardy-Weinberg Equilibrium equation, where heterozygotes are represented by the 2pq term.
Therefore, the number of heterozygous individuals (Aa) is equal to 2pq which equals
2 × 0.9 × 0.1 = 0.18
Thus, the frequency of heterozygote is 0.18, while the percentage distribution in the population is 18%
Amount of wear, and how long they are may contribute with age and maybe even coloration and pigment.
