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A genetic defect of the CFTR gene affects how the cells in the body distribute sodium. There are different mutations, but all allow too much sodium to leave the cell. Thus, the mucus in a person with cystic fibrosis loses it's fluidity and becomes very thick.
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What are the internal secretions of the body if you have cystic fibrosis?
Cystic Fibrosis patients has a sticky mucus that clogs the lungs, causes lungs infections, obstructs the pancreas, and stops natural enzymes that helps the body break down food.
Why do chloride ions build up outside certain cells in the patients with cystic fibrosis?
In cystic fibrosis, mutations in the CFTR gene prevent chloride ions from exiting cells properly. This leads to a buildup of chloride ions outside certain cells, causing a thick mucus to form in the airways and other organs.
FActs about Cystic Fibrosis?
it causes unusually thick mucus in the pancreas
What disease causes mucus build up in lungs?
Cystic Fibrosis
What type of genetic disorder occurs when the body produces abnormally thick mucus?
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.
An immune disorder in which the airways constrict and become clogged with mucus is?
cystic fibrosis
What disorder cause abnormally thick mucus in lungs and intestines?
cystic fibrosis
What is the most common lethal genetic disease in US African Americans?
Cystic fibrosis it is characterized by thick mucus in the lungs
A disorder in which the body produces abnormally thick mucus in the lungs and intestines is called?
Cystic fibrosis is a genetic disorder that causes the body to produce thick and sticky mucus in the lungs and digestive system. This can lead to respiratory problems, digestive issues, and other complications. Early diagnosis and management are crucial in improving quality of life for individuals with cystic fibrosis.
What is the sequence of amino acid in cystic fibrosis?
The sequence of amino acids in cystic fibrosis is caused by a mutation in the CFTR gene, which leads to the production of a faulty cystic fibrosis transmembrane conductance regulator protein. This mutated protein results in abnormal function, leading to the characteristic symptoms of cystic fibrosis such as thick mucus production.
What are symptoms of cystic fibrosis?
the symptoms of cystic fibrosis are has chesty coughs and feeling very flemmy. struggling to breath can also be a sign and mucus will fill the lungs and cover the throat.
Which condition causes thick mucus to form in the lungs pancreas and intestines?
Cystic fibrosis
