Preview

Cystic Fibrosis Case Study

Good Essays
Open Document
Open Document
277 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Cystic Fibrosis Case Study
1. Describe the symptoms of cystic fibrosis.

The different symptoms of cystic fibrosis include repeated infections and thick mucus secretions in the lungs, it affects you with wheezing, a chronic cough, bronchitis, asthma, weight loss, dehydration, and many more mainly affecting the lungs and stomach. Sufferers may also feel very fatigued easily.

2. Describe two problems associated with the presence of thick, sticky mucus
(a) in the lungs and breathing passageways
(b) in the digestive system

a) The problems associated with thick sticky mucus in the lungs and breathing passageways are frequent respiratory infections and breathing difficulties.
b) The problems associated with thick sticky mucus in the digestive system is malnutrition,


You May Also Find These Documents Helpful

  • Good Essays

    The fluid makes it harder to expand the lungs because the fluid makes the alveoli sticky and unable to open/expand.…

    • 760 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Chronic bronchitis B. Bronchial Asthma * Recurrent and reversible shortness of breath * Occurs when the airways of the lungs become narrow as a result of: * Bronchospasms * Inflammation of the bronchial mucosa * Edema of the bronchial mucosa * Production of viscid mucus * Alveolar ducts/alveoli remain open, but airflow to them is obstructed * Symptoms * Wheezing * Difficulty breathing C. Asthma *…

    • 5705 Words
    • 23 Pages
    Good Essays
  • Better Essays

    Unit Project 4

    • 1226 Words
    • 5 Pages

    Lungs – Mucus plugging, chronic bacterial infections, pronounced inflammatory response, damaged airways leading to respiratory insufficiency, progressive decline in pulmonary function.…

    • 1226 Words
    • 5 Pages
    Better Essays
  • Satisfactory Essays

    Cystic Fibrosis

    • 336 Words
    • 2 Pages

    Question One: The physician asked the mother of the infant if the infant's skin was salty because one of the symptoms of cystic fibrosis is having thick and heavy mucous ... and salty sweat. When the CFTR (Cystic Fibrosis Trans membrane Conductance Regulator) protein is defective, epithelial cells can't regulate the way chloride (part of the salt called sodium chloride) passes across cell membranes. This disrupts the essential balance of salt and water needed to maintain a normal thin coating of fluid and mucus inside the lungs, pancreas, and passageways in other organs.…

    • 336 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    Cystic Fibrosis is a life threatening condition that causes severe damage to the lungs and digestive system. Developing this condition can change a person's entire life. Depending on the severity of the condition a person can be affected by mild symptoms such as shortness of breath, all the way to severe symptoms such as rectal prolapse, or even death. Screening is done on infants in all 50 states; therefore if a child has inherited Cystic Fibrosis it will be known in the first months of life. As professional staff members of a nursing community it will be necessary to help prepare the child and the family for the life of Cystic Fibrosis.…

    • 802 Words
    • 3 Pages
    Good Essays
  • Satisfactory Essays

    Cystic fibrosis is a genetic disease, and it is inherited by autosomal recessive, which means that there must be two copies of an abnormal gene and it has to be present in order for the disease or trait to develop. While I was learning about autosomal recessive, I learned that gene’s come in pairs and both pairs must be defective to cause a disease. As I looked deeper into Cystic fibrosis I learned that it affects the respiratory system and also the digestive system. This disease is a defect in the chromosome 7, chromosome 7 is also known as CFTR or cystic fibrosis transmembrane conductance regulator. Like most diseases these days the way it affects someone or shows in someone depends on the severity of the disease. For instance, the way cystic fibrosis shows in a child may be completely different compared to someone in there later ages. For the most part the symptoms are always the same for both the respiratory and the digestive system. When it comes to the respiratory system the symptoms that you need to look for is a constant cough that produces a lot of mucus, Wheezing or feeling breathlessness. Always having a stuffy nose and not being able to exercise the way you may want too is also a symptoms due to the respiratory system. As you can tell from the…

    • 960 Words
    • 3 Pages
    Satisfactory Essays
  • Good Essays

    1. What are the symptoms of cystic fibrosis and PKU with respect to the digestive system?…

    • 923 Words
    • 4 Pages
    Good Essays
  • Good Essays

    Cystic fibrosis is an inherited disease of secretory glands, including the glands that make mucus and sweat. "Inherited" means that the disease is passed through the genes from parents to children1, 2. People who have cystic fibrosis inherit two faulty cystic fibrosis genes one from each parent. The parents likely don't have the disease themselves. Cystic fibrosis mostly affects the lungs, pancreas, liver, intestines, sinuses, and sex organs. Mucus is a substance made by the lining of some body tissues. Normally, mucus is a slippery, watery substance3, 4. It keeps the linings of certain organs moist and prevents them from drying out or getting infected. However, if have cystic fibrosis, mucus becomes thick and sticky. The mucus builds up in lungs and blocks airways, the tubes that…

    • 345 Words
    • 2 Pages
    Good Essays
  • Good Essays

    Symptoms are nonexistent for carriers of the disease. Cystic Fibrosis produces an abnormal amount of thick, sticky mucus within the lungs, airways and digestive system. This inhibits proper oxygen flow and initiates infections as well as trapping bacteria in the lungs (irreversible). Digestive functions of the pancreas are also impaired.…

    • 631 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Some respiratory signs include thick salty mucus clogging the tubes that carry air in and out of our lungs. This can cause, a persistent cough that produces mucus, wheezing, breathlessness, and repeated lung infections. Respiratory complications include, bronchiectasis, chronic infections, nasal polyps, pneumothorax, collapsed lung, respiratory failure and coughing up…

    • 933 Words
    • 4 Pages
    Good Essays
  • Good Essays

    Cystic Fibrosis

    • 569 Words
    • 3 Pages

    Symptoms and complications related to the lungs and sinuses can include, increased mucus in the sinuses or lungs, coughing, and pneumonia. Severe sinus pain or pressure can be caused by infection or nasal polyps. Symptoms and…

    • 569 Words
    • 3 Pages
    Good Essays
  • Good Essays

    This disease is caused by a mutation in a gene causing the body to produce excess amounts of mucus, that then builds up and creates difficulty in breathing and digestion (Cystic). Symptoms vary based on the function they affect such as bowels, or lungs and sinuses. Weight loss, fatigue, fever, loss of appetite, shortness of breath, increased gas and bloating, and severe constipation are just a few of the many serious symptoms of cystic fibrosis. Cystic fibrosis can start as early as newborns causing them delayed growth, lack of bowel movements in up to the first 48 hours of life, and salty-tasting skin. High salt levels found in perspiration can be a good indicator of the disease…

    • 955 Words
    • 4 Pages
    Good Essays
  • Powerful Essays

    Copd

    • 5954 Words
    • 24 Pages

    As inflammation continues, the airways constrict, becoming excessively narrow and swollen. This leads to excess mucus production and poorly functioning cilia, a combination that makes airway clearance especially difficult. When people with COPD can't clear their secretions, they develop the hallmark symptoms of COPD, including a chronic, productive cough, wheezing and dyspnea. Finally, the build-up of mucus attracts a host of bacteria that thrive and multiply in the warm, moist environment of the airway and lungs. The end result is further inflammation, the formation of diverticula (pouch-like sacs) in the bronchial tree, and bacterial lung infection, a common cause of COPD exacerbation.…

    • 5954 Words
    • 24 Pages
    Powerful Essays
  • Better Essays

    Spending a lot of their time in the hospital setting, they decided to make the most of it. Their parents raised them to look at their disease as an opportunity and a challenge. The twins were determined to beat the odds. And beat the odds they did. Isabel and Anabel grew up with a very strong support group. Their parents were always their for them and exposed them to other kids their age struggling with Cystic Fibrosis. They talked about going to camps every summer that were specifically for kids with Cystic Fibrosis. Throughout the years, the twins have met many doctors and nurses who have helped educate and motivate them through this challenging journey. Having this illness has really opened their eyes to the fact that they still have healthy minds, to not take advantage of the time they have on this earth, and that they are more than their bodies. Accepting and letting go of the fact that they have Cystic Fibrosis and will have it forever was the first step to a motivated and positive mindset. The twins strongly believe that they can do anything they set their minds…

    • 1477 Words
    • 6 Pages
    Better Essays
  • Satisfactory Essays

    Cystic fibrosis has been a major part of not only my life , but my families’ lives too. I have two sisters , my twin Alani, and my oldest sister Adriana ,who also suffer from cystic fibrosis . Our family supports us everyday to help fight this disease .…

    • 135 Words
    • 1 Page
    Satisfactory Essays