Cystic Fibrosis Research Paper

Superior Essays
Cystic Fibrosis is an inherited disease of the secretory glands, glands that make up mucus and sweat. It is also known as mucoviscidosis, that affects mostly the lungs but also the pancreas, liver, kidneys and intestine. Long term issues include difficulty breathing and coughing up sputum as a result of frequent lung infections. A defect in the CFTR gene causes cystic fibrosis. This gene makes a protein that controls the movement of salt and water in and out of your body's cells. In people who have CF, the gene makes a protein that doesn't work well. This causes thick, sticky mucus and very salty sweat.
Research says that the CFTR protein also affects the body in other ways. This may help explain other symptoms and complications of CF.
More
…show more content…
However, they can pass the faulty CFTR gene to their children.
The image below shows how two parents who are both CF carriers can pass the faulty CFTR gene to their children. Cystic fibrosis affects both males and females and people from all racial and ethnic groups. However, the disease is most common among Caucasians of Northern European
…show more content…
They're related to how CF affects the respiratory, digestive, or reproductive systems of the body. In the respiratory system sticky mucus builds up in their airways. This buildup of mucus makes it easier for bacteria to grow and cause infections. Infections can block the airways and cause frequent coughing that brings up thick spit or mucus that is sometimes bloody.
People who have CF tend to have lung infections caused by unusual germs that don't respond to standard antibiotics. Lung infections caused by bacteria called mucoid pseudomonas are much more common in people who have CF than in those who don't. An infection caused by these bacteria may be a sign of CF.
People who have CF have frequent bouts of sinusitis, an infection of the sinuses. The sinuses are hollow air spaces around the eyes, nose, and forehead. Frequent bouts of bronchitis and pneumonia also can occur. These infections can cause long-term lung damage.
In the digestive system mucus can block tubes, or ducts, in your pancreas. These blockages prevent enzymes from reaching your

Related Documents

  • Great Essays

    Common symptoms are chronic coughing, recurring chest colds, wheezing, and shortness of breath. The main reason that they have respiratory tract infections is because they have a problem with mucus control in their respiratory tract. This can cause a lot of problems if the mucus isn’t removed. For example the mucus can pool in the lungs and it is also a perfect environment for bacteria to grow. Normally the mucus would be alleviated through the cilia, but because of all the back up of mucus it becomes clogged.…

    • 1413 Words
    • 6 Pages
    Great Essays
  • Decent Essays

    Website: http://www.wsvn.com/story/26299941/camps-take-cystic-fibrosis-patients-surfing Cystic fibrosis (CF) is a genetic-disease that causes thick, sticky mucus to build up in the lungs, digestive tract, and continues throughout other areas of the body. Cystic fibrosis has signs and symptoms that differs, depending on how bad the disease affects someone. Cystic fibrosis varies through ages, it affects infants, teenagers, and young adults, but is mostly found in white people.…

    • 378 Words
    • 2 Pages
    Decent Essays
  • Improved Essays

    People who are prone to delta F508 mutation tend to have more critical symptoms of cystic fibrosis because of the lack of chloride ion transport, needed to control the thin layer of mucus that can be removed by the cilia lining the lungs and organs. The lack of chloride ion transport causes a thick mucus layer that the cilia can not remove, which in result traps bacteria causing disease. The chloride channels are to let chloride out of the epithelium cells. Someone who does that have cystic fibrosis the channels will open a fair amount of times in order to keep it balanced inside and outside of the cells,…

    • 390 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    The mucus becomes unmanageable leading to complications with the lungs, pancreas, liver, salivary glands, and testes. The copious accumulations of the person’s secretion than clogs the airway of the lungs and glandular tissues…

    • 657 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    Since the discovery of the gene, doctors have been trying to to create effective therapies to treat Cystic Fibrosis. One of the doctors who works at the Sick Kids Hospital in Toronto, and studies the cystic fibrosis gene said, “Finding the gene opened the door to unprecedented knowledge of the disease. After its discovery we were able to study and understand how the protein made by the CFTR gene worked and what happened when it didn’t, Once we figured this out, therapy that targeted defects caused by CF gene mutations could begin” (Doctor Christine Bear). The discovery of the Cystic Fibrosis gene has helped the doctors learn much more about the disease and hopefully will help them find a cure to Cystic Fibrosis in the…

    • 1160 Words
    • 5 Pages
    Improved Essays
  • Improved Essays

    In Cystic Fibrosis, symptoms start slowly. The respiratory tract (nose to lungs) and the gastrointestinal (digestive) systems are the most affected. Symptoms usually start in the gastrointestinal system. Male fertility and sweat glands are also affected. Only about fifteen percent of babies who carry the disease have meconium ileus which is sticky and thick caused by thick mucus from intestinal glands.…

    • 413 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Genetic Disorder Paper Cystic fibrosis is a progressive, genetic disease that causes persistent lung infections and limits the ability to breathe over time (cystic fibrosis foundation). It is a decease in the secretory glands, the glands that make mucus and sweat (medicine). It causes the cells in those parts to not function correctly and when needed to produce fluids, produce thick, sticky mucus in the lungs, pancreas and other organs (cystic fibrosis foundation). It builds up and blocks tubes and airways making it harder to breathe.…

    • 614 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    Cystic Fibrosis Presentation Cystic fibrosis is genetic disorder. It is an inherited disorder that can result in a severe damage to the respiratory and digestive systems. This disorder can affect the lungs, pancreas, intestines, liver and even the sex organs. Cystic fibrosis builds up a thick and sticky mucus in the lungs and other respiratory and digestive organs in our body. For an infant to be at risk of developing Cystic Fibrosis, both parents must pass on the abnormal gene to the infant.…

    • 905 Words
    • 4 Pages
    Improved Essays
  • Decent Essays

    Cystic Fibrosis was first discovered in 1938 by Dr. Dorothy Hansine Andersen, she described the characteristics of the disease of the pancreas, lungs, and other organs, but this was not much information to go on from. She later discovered more information on Cystic Fibrosis in 1949, she found out it was caused by a recessive mutant gene. Cystic Fibrosis(CF) is a thick and sticky mucus that clogs the airways, making it hard to breathe and causing damage. It is caused by a defect in a gene that changes a specific protein that regulates the movement of salt in and out of cells at birth. In order for someone to be diagnosed with CF, the child would need to get one copy of the gene from both parents.…

    • 523 Words
    • 3 Pages
    Decent Essays
  • Improved Essays

    Cystic fibrosis can also cause intestinal malabsorption, which can lead to severe malnutrition to the individual and growth failure. Cystic fibrosis can lead to death if untreated from and early childhood. (Campbell., 2012) This genetic disease is caused by mutation in a pair of genes which are located on chromosome 7 called CFTR, which stands for “Cystic fibrosis transmembrane conductance regulator”. Unlike the sex cells, every cell in the human body has 46 chromosomes, because 23 pairs of chromosomes are inherited from the mother as well as the…

    • 836 Words
    • 4 Pages
    Improved Essays
  • Improved Essays

    With Cystic Fibrosis mucus is thick which causes passageways…

    • 495 Words
    • 2 Pages
    Improved Essays
  • Superior Essays

    During the 1930’s and 40’s, the majority of children diagnosed with Cystic Fibrosis died in the first couple years of their lives. ("Prognosis") This unfortunate reality is caused by the effect of the inherited disease, Cystic Fibrosis; this sickness is caused by the build-up of excess mucus that has the potential to permanently damage one’s lungs. Cystic Fibrosis, also known as CF, Cystic Fibrosis of Pancreas, Fibrocystic Disease of Pancreas, or Mucoviscidosis, is a non-contagious genetic disease that works by producing mucus that is abnormally thick and sticky, and can ultimately kill the patient. Mucus, as most are aware of, is a slippery substance that lubricates and protects the linings of the airways, digestive system, reproductive system,…

    • 1584 Words
    • 7 Pages
    Superior Essays
  • Improved Essays

    Cystic fibrosis (CF) is a lifelong, hereditary disease that causes thick, sticky mucus to form in the airways, causing lung damage, making it hard to breathe, and leading to serious lung infections. In the pancreas, it clogs the pathway leading to the digestive system, interfering with proper…

    • 1065 Words
    • 5 Pages
    Improved Essays
  • Improved Essays

    Chronic obstructive pulmonary disease is a lung disease that causes inflammation and stops the airflow from the lungs. Symptoms such as cough, sputum and wheezing are related to this condition. The main cause of the disease is cigarette smoke and exposure to irritating gases for a long time. People with COPD are at a much higher risk of developing heart diseases and other conditions. Contributing conditions to COPD are emphysema and chronic bronchitis.…

    • 751 Words
    • 4 Pages
    Improved Essays
  • Great Essays

    It is very common in our society with 1200 of the 70,000 affected worldwide living in Ireland (Cystic Fibrosis Ireland, 2014). CF causes the body to produce thick sticky mucus that blocks the lungs and causes lung infections. CF also stops the body for producing pancreatic enzymes which are necessary for breaking down and absorbing food. There are various symptoms of CF including, salty skin, persistent coughing often with phlegm, lung infections, shortness of breath, poor growth and weight gain and heavy stools or difficulty with bowel movements (Cystic Fibrosis Ireland, 2014). CF is caused by a gene that is passed from parent to child.…

    • 2133 Words
    • 9 Pages
    Great Essays