Cystic Fibrosis Questions And Answers? All Answers

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Cystic Fibrosis| NCLEX Rn exam practice questions with answers

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What can cystic fibrosis be mistaken for?

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So, cystic fibrosis was often misdiagnosed as something else, such as whooping cough, chronic bronchitis, or asthma. It was not officially described for the medical community until 1933.

Is there a disease similar to cystic fibrosis?

PCD is easy to confuse with cystic fibrosis because the two genetic diseases have similar effects on the lungs. In both disorders, mucus accumulates in patients lungs, causing frequent infections and severe congestion.

Can you be misdiagnosed with cystic fibrosis?

On reassessment of 179 children who had previously been diagnosed as having cystic fibrosis seven (4%) were found not to have the disease. The importance of an accurate sweat test is emphasised as is the necessity to prove malabsorption or pancreatic abnormality to support the diagnosis of cystic fibrosis.

What lung disease is similar to cystic fibrosis?

Bronchiectasis is sometimes called non-cystic fibrosis bronchiectasis. This is because there is a different condition called cystic fibrosis. People who have cystic fibrosis can have lung symptoms similar to those of bronchiectasis, but the treatments and outlook are different.

How do you rule out cystic fibrosis?

A sweat test checks for high levels of chloride in your sweat. The sweat test is the standard test for diagnosing cystic fibrosis. It may be used if you have symptoms that may indicate cystic fibrosis or to confirm a positive diagnosis from a screening of your newborn baby.

What are some questions to ask about cystic fibrosis?

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What questions should I ask about cystic fibrosis?

Can my child with CF be around another child with CF? Can a lung transplant cure CF? What medication does my child need and are there any side-effects? Do people with CF need their treatment daily or can they skip days?

What are 3 interesting facts about cystic fibrosis?

What is the major problem in cystic fibrosis?

The most serious and common complications of cystic fibrosis are problems with the lungs, also known as pulmonary or respiratory problems, which may include serious lung infections.

What can cystic fibrosis be mistaken for?

So, cystic fibrosis was often misdiagnosed as something else, such as whooping cough, chronic bronchitis, or asthma. It was not officially described for the medical community until 1933.

Which parts of the body are most affected by cystic fibrosis?

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Cystic fibrosis (CF) is an inherited disorder that causes severe damage to the lungs, digestive system and other organs in the body. Cystic fibrosis affects the cells that produce mucus, sweat and digestive juices. These secreted fluids are normally thin and slippery.

What parts of the body does cystic fibrosis affect?

Cystic fibrosis (CF) is an inherited disorder that causes severe damage to the lungs, digestive system and other organs in the body. Cystic fibrosis affects the cells that produce mucus, sweat and digestive juices.

Where is cystic fibrosis most common?

The cystic fibrosis gene is most common in Caucasians of northern European descent. The disease occurs most frequently in these people, but can occur in any ethnic population.

What are 3 interesting facts about cystic fibrosis?

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What are 2 interesting facts about cystic fibrosis?

There are close to 40,000 children and adults living with cystic fibrosis in the United States (and an estimated 105,000 people have been diagnosed with CF across 94 countries). Approximately 1,000 new cases of CF are diagnosed each year. More than 75 percent of people with CF are diagnosed by age 2.

What are 5 facts about cystic fibrosis?

Whats unique about cystic fibrosis?

Cystic fibrosis affects the cells that produce mucus, sweat and digestive juices. These secreted fluids are normally thin and slippery. But in people with CF, theyre thick and sticky. Instead of acting as lubricants, these secretions plug up the tubes, ducts and airways in your body.

What race gets cystic fibrosis the most?

Cystic fibrosis is most common among Caucasians. In the U.S., the chances of being a carrier of a CFTR mutation are: 1 in 29 Caucasian-Americans. 1 in 46 Hispanic-Americans.

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