What Is The Primary Characteristic Of Cystic Fibrosis?

Which of the following is characteristic of cystic fibrosis?

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..

Can cystic fibrosis go undetected?

While cystic fibrosis is usually diagnosed in childhood, adults with no symptoms (or mild symptoms) during their youth can still be found to have the disease.

Can you have a mild form of cystic fibrosis?

Atypical CF is a milder form of the CF disorder, which is associated with mutations of the cystic fibrosis transmembrane receptor gene. Instead of having classic symptoms, individuals with atypical CF might only have mild dysfunction in 1 organ system and might or might not have elevated sweat chloride levels.

How does cystic fibrosis affect you emotionally?

People with chronic diseases, such as cystic fibrosis, are at greater risk for developing clinical depression. When left untreated, depression can interfere with your ability to manage your CF effectively and experience a better quality of life.

Are there different types of cystic fibrosis?

Are there different types of cystic fibrosis? There are over 2,000 identified mutations of the cystic fibrosis gene. Cystic fibrosis is a very complex condition that affects people in different ways. Some suffer more with their digestive system than the lungs.

How Cystic fibrosis affects daily life?

Cystic fibrosis affects the respiratory tract because a person with the condition produces thicker mucus in their lungs than is normal in a healthy body. Some people with cystic fibrosis may also experience constant coughs, wheezing, and reduced lung function that makes breathing difficult.

What are the main physical impacts of cystic fibrosis?

These symptoms include poor lung function, frequent and persistent lung infections and the inability to effectively digest food, particularly fats. Additional complications include CF-related diabetes, bone disease and infertility. Find out more about the symptoms of cystic fibrosis.

What are the 3 most common types of mutations that cause cystic fibrosis?

The most recent classification system groups mutations by the problems that they cause in the production of the CFTR protein:Protein production mutations (Class 1)Protein processing mutations (Class 2)Gating mutations (Class 3)Conduction mutations (Class 4)Insufficient protein mutations (Class 5)

What race is cystic fibrosis most common in?

Cystic fibrosis is a common genetic disease within the white population in the United States. The disease occurs in 1 in 2,500 to 3,500 white newborns. Cystic fibrosis is less common in other ethnic groups, affecting about 1 in 17,000 African Americans and 1 in 31,000 Asian Americans.

What part of the cell is affected by cystic fibrosis?

CF affects a cell protein called CFTR (cystic fibrosis transmembrane regulator). CFTR controls the flow of water and certain salts in and out of the body’s cells. As the movement of salt and water in and out of cells is changed, the mucus that many cells normally make gets thicker.

How Cystic fibrosis affects the digestive system?

About 90 percent of people with CF have sticky mucus that blocks ducts in the pancreas and prevents enzymes from reaching the small intestine to digest food. Undigested food in the intestines can cause pain, cramping, gas and either loose, greasy, floating stools or constipation and blockages.

What is life like with cystic fibrosis?

Living with cystic fibrosis comes with many challenges, including medical, social, and financial. By learning more about how you can manage your disease every day, you can ultimately help find a balance between your busy lifestyle and your CF care. People with CF are living longer, healthier lives than ever before.