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There are no 'Side Effects', just things that 'come with the package'. You can suffer breathlessness, bowel problems and probalmes with liver and kidneys. There are other things too, but at age 13, that's all I've really had so far.
Tin cans doesn't affect the amount of dissolved oxygen in waters.
Oxygen cycle does not affect. It is because the ozone is located in stratosphere.
DEATH
more oxygen
fibrosis woks on you digestion system in your body.
Yes they are. Is that your question?
There are no 'Side Effects', just things that 'come with the package'. You can suffer breathlessness, bowel problems and probalmes with liver and kidneys. There are other things too, but at age 13, that's all I've really had so far.
The mucus that forms from cystic fibrosis affects the gas exchange in humans. The build up from cystic fibrosis can affect the gas exchange by increasing carbon dioxide and decreasing oxygen.
The genotype would have to be homozygous recessive if the child was completely effected by the disease. The "normal" paretns would have to have heterozygous recessive genotypes. This makes sense since the allele that causes sickle cell shows incomplete dominance when present with a normal allele in a pair. The "normal" parents actually would have a mixture of sickle cell shaped red blood cells combined with normal shaped ones. The carrier parents does not display symptoms of the disease since the regular red blood cells alone can fill the body's need for oxygen under normal circumstances. The only time the cArrier would notice would be under times of extreme oxygen demand, such as a sprint.
yes
A build up of mucus in the lungs, with the 'victim' continuously needing to be hit on the back until the mucus is coughed up, someone with the disease can live a perfectly normal life with a life expectancy of around 50 years.
There are a few things that can cause you to have insufficient oxygen. Lung disease, asthma, pulmonary hypertension, lung fibrosis or lung cancer to name a few.
If it is COPD emphysema pulmonary fibrosis... Its preventing the disease from getting worse and comfort actions. quit smoking. albuterol inhalers to help open the lungs inhaled steroids like advair to reduce inflamation. sometimes lung transplant is an option. Asthma- knowing triggers and preventing attacks. albuterol when there is an attack. advair if chronic breathing issues. Cystic fibrosis- antibiotic therapy. mucus clearing therapy, transplant. chronic bronchitis- quit smoking . albuterol. oxygen
It raises the temperature as your blood vessels are getting less oxygen.
Oxygen tanks can help manage symptoms of pulmonary fibrosis by providing extra oxygen to the lungs, but they do not prevent mortality from the disease. Pulmonary fibrosis is a progressive condition, and while oxygen therapy can improve quality of life and alleviate symptoms, it does not cure the underlying disease. Treatment strategies for pulmonary fibrosis focus on addressing the underlying cause, managing symptoms, and improving quality of life.
There are many, many examples. The following are completely arbitrary: For instance, the most abundant protein in the blood is albumin, which is also the chief protein of egg whites. Another example is titin, the largest naturally occurring protein currently known. Hemoglobin is a major protein studied in biochemistry. It is involved in the transport of oxygen and carbon dioxide in the blood. The cystic fibrosis transmembrane conductance regulator (CFTR) is a protein channel that is defective in the disease cystic fibrosis.