Cystic Fibrosis
The nervous system
cystic fibrosis
Cystic fibrosis affects the respiratory, digestive, and reproductive systems.
CFTR gene stands for Cystic Fibrosis Transmembrane Conductance Regulator gene. It is responsible for encoding a protein that regulates the flow of ions across cell membranes, particularly in the lungs and digestive system. Mutations in this gene can lead to cystic fibrosis, a genetic disorder affecting the lungs and digestive system.
Adequate protein intake is important for individuals with cystic fibrosis to support growth, development, and maintenance of muscle mass. Protein also plays a role in fighting infection and supporting the immune system, both of which are particularly important in managing the symptoms of cystic fibrosis. However, excessive protein intake is not recommended, as it can put additional strain on the kidneys.
Yes, cystic fibrosis (CF) can affect multiple systems in the body. It primarily impacts the lungs, but it can also affect the digestive system, pancreas, liver, and reproductive system. CF can lead to complications in these areas, requiring comprehensive care from a multidisciplinary healthcare team.
Our lab works on site-specific recombinases, we are in the process of developing a system to cure genetic diseases of which cystic fibrosis is also a part of our major goal to be achieved.
Cystic fibrosis is a chronic genetic disease. It is not an autoimmune disease. However, recent research indicates that an overactive immune response contributes to inflammation and damage in the lungs.
Cystic fibrosis causes thick mucus to build up in the lungs, making it difficult to breathe and reducing oxygen absorption. The disease also affects the pancreas, which results in poor absorption of nutrients from food. This can lead to malnutrition and weight loss in individuals with cystic fibrosis.
According to the Cystic Fibrosis Trust's website:Cystic Fibrosis (CF) is one of the UK's most common life-threatening inherited diseases.Cystic Fibrosis affects over 9,000 people in the UK.Over two million people in the UK carry the faulty gene that causes Cystic Fibrosis - around 1 in 25 of the population.If two carriers have a child, the baby has a 1 in 4 chance of having Cystic Fibrosis.Cystic Fibrosis affects the internal organs, especially the lungs and digestive system, by clogging them with thick sticky mucus. This makes it hard to breathe and digest food.Each week, five babies are born with Cystic Fibrosis.
Cystic fibrosis is the genetic disorder that occurs when the body produces abnormally thick mucus. This condition affects the lungs, digestive system, and other organs, leading to recurrent infections and difficulty in breathing and digesting food.