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Cystic fibrosis affects the respiratory, digestive, and reproductive systems.
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How does cystic fibrosis affect the urinary system?
Cystic fibrosis primarily affects the respiratory and digestive systems, but it can also have implications for the urinary system. The thick mucus characteristic of the disease can lead to complications in the kidneys, such as kidney stones or urinary tract infections, due to dehydration and imbalances in salt and fluid levels. Additionally, cystic fibrosis can result in reduced kidney function over time, complicating the body's ability to regulate electrolytes and maintain fluid balance. However, the urinary system is generally less affected than other systems in cystic fibrosis.
If you have cystic fibrosis what internal secretion of the body becomes thick and sticky?
If you have cystic fibrosis what internal secretion of the body becomes thick and sticky?
Is cancer a growth disorder of cells that occurs when cells divide uncontrollably within the body or is it cystic fibrosis?
(Cystic fibrosis/Cancer) is a growth disorder of cells that occurs when cells divide uncontrollably within the body.
What parts of the body are affected by cystic fibrosis?
airways, bronchial, lungs, pancreas, skin, liver, small instestine, reproductive tract
is cystic fibrosis affect the human body?
Cystic fibrosis is widely recognized as a lung disease, but it is actually a disease that affects many parts of the body. So yes. it can:) hope this is helpful
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 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.
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.
When Body Produces abnormally thick mucus when a person has a this genetic disorder?
Cystic fibrosis
What two parts of the body are affected by cystic fibrosis?
cystic fibrosis means there is too much fluid in the lungs and it makes it very hard for them to breathe. It also affects their growing and their digestive system because of the mucus. Unfortunately even a small cold can make them very sick because it affects the lungs. Unfortunately they usually die in their 30's and it is a very serious disease that more people need to be educated about.
How can cystic fibrosis cause problems with absorption of food and oxygen?
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.
What is cystic fibrosis gene disorder?
The genes on each chromosome control specific functions of the human body. The gene on chromosome 7 produces a protein called cystic fibrosis transmembrane regulator. Mutation in the DNA level of chromosome 7 leads to the absence of this protein which leads to cystic fibrosis. Cystic fibrosis is a recessive disease. It means that both copies of the gene must be defective. An affected person will have abnormal cystic fibrosis transmembrane regulator gene on each chromosome 7. Therefore both biological parents must have an abnormal gene. One abnormal copy is inherited from each parent. A person with one normal gene and one abnormal gene is called a cystic fibrosis carrier. Cystic fibrosis carriers do not show any symptoms but they may pass the abnormal gene to their children. Therefore the parents can be either cystic fibrosis carriers or affected themselves.
