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Q: In patients with CF how can you lower CO2 levels?
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Continue Learning about General History

When was Palamós CF created?

Palamós CF was created in 1898.


When was Vinaròs CF created?

Vinaròs CF was created in 1965.


When was Alondras CF created?

Alondras CF was created in 1951.


When was Cádiz CF created?

Cádiz CF was created in 1910.


When was Muleño CF created?

Muleño CF was created in 1989.

Related questions

How many cf in 7 lb of co2?

The answer depends on the temperature and pressure.


Will Carbon Dioxide Fall from Warm Air?

No. If anything, the warmer the air, the more turbulent it is, more thoroughly mixing CO2. Sometimes in caves and mine shafts, where the air is very still, CO2 settles out into fairly high concentrations. Bats can survive CO2 levels more than a hundred times higher than what is lethal to people. But in general, once CO2 gets into the air the only thing that pulls it back out is the sequestration activity of photosynthetic organisms. Cf. Azolla Event.


How do 1 Solve for quartiles in a grouped data?

formula in solving quartiles: QK = ([kN - <CF] / FQK)i where in: Q = Quartile k = given value N = Total number of variables <CF = Lower Frequency of Lower Area i = Interval


What is a closed angle glaucoma?

bv cf cf cf cf cf cf cfgrertrgsghsh


Cystic Fibrosis causes what?

CF is a genetic disorder. In order for a child to have CF, 2 recessive alleles must be present. Only two CF carriers can produce offspring with CF, only there is a 25% chance that the offspring has CF. CF carriers DO NOT have CF, but have the gene that causes it (like birds that carry West Nile).It's a genetic disease where patients affected have both of the two copies of the gene CFTR with mutation inactivating the gene. It brings to the formation of a CFTR protein with absent or decreased function. The CFTR is a transmembrane channel that transport chlorine ions (Cl-), so the patients affected have an abnormous concentration of Cl- on the mucose leadind to an increased viscosity of mucus that causes problems expecially at the lungs and pancreas, and to the reproductive apparatus. The average life of CF patients is very decreased. The gravity of the symptoms variate from patient to patient and it depends on the kind of mutations present, so there are severe forms, mild and light forms.cystic fibrosis is an inherited disease which means you can only get the disorder passed on to you from your parents. However because the CF allele is recessive both parents have to be carriers and even then there is a 25% chance of inheritance


Discuss the effects of carbon tetrachloride toxicity?

Cf. "Related links" at the lower left corner of this answer page.


What is special about ough?

The letters ough have 10 different pronunciations."through" (cf. true)."thought" (cf. taut)."though" (cf. toe)."cough" (cf. coffin)."rough" (cf. ruffian)."bough" (cf. to bow)."thorough" (cf. about) [British English].


Should you go out with a guy who has Cystic Fibrosis?

Cystic fibrosis is noncommunicable, so in that respect there is no concern. If you want to have children then there is about a 50% chance your kids will have CF, there is genetic screening to determine if your also a carrier, thus raising the chance. CF is most common in white Europeans especially of German descent. With early identification and tratment the outlook for a long life for CF patients is better than ever.


What does cf mean in text messaging?

Cf


When was Palencia CF created?

Palencia CF was created in 1960.


What is the chemical formula for CF?

The chemical formula for CF is carbon monofluoride.


Are Purple fingertips in cystic fibrosis patience normal?

Yes, the finger nails are often bluish in patients with Cystic Fibrosis. Clubbing of the fingernails is also seen in later stages of CF. My daughter had CF for 34 years before dying of Sepsis (blood infection), 115 days after a double lung transplant.