Taking a Look at Cystic Fibrosis - 660 Words

There are many diseases that greatly affect our respiratory physiology; one of those diseases is cystic fibrosis. Cystic fibrosis, according to the National Institute of Health (2013), is an inherited disease of the secretory glands or exocrine glands. Not only does this disease affect our respiratory system, it takes a toll on our digestive system. The respiratory system includes the gas exchange from our external atmosphere and our internal environment. This gas exchange of oxygen and carbon dioxide through our atmosphere and lungs does play a roll with cystic fibrosis. Cystic fibrosis is inherited, it affects many parts of the body mainly the respiratory system, and there are many signs and symptoms to this overwhelming disease. The respiratory system is the body’s source for breathing. Without our respiratory system, gas exchange would not be able to occur. Inhaling oxygen and exhaling carbon dioxide. In our respiratory system our upper airways and bronchi can be said to warming, humidifying, and filtering inspired air. By warming the air inhaled it will not cause damage to our internal environment which is body temperature, with warming the air that is inhaled cold air will reach that body temperature, humidifying our body through inhalation of oxygen, our epithelial cells remain moist and do not dry out (Silverthorn, 2013), and finally the mucus that is in our pharynx come upon many inhaled microorganisms and/or other pathogens. As Silverthorn (2013) states, mucusShow MoreRelatedTaking a Look at Cystic Fibrosis733 Words   |  3 PagesCystic fibrosis is life threatening, progressive and genetic disorders that cause severe damage to the lungs and digestive systems. About 30,000 children’s and adults in the United States are affected by this chronic disease. Cystic fibrosis is an inherited condition which affects the body’s exocrine glands (mucus secretion glands). The secreted fluids such as mucus, sweat and digestive juices are normally thin and slippery. The secretions become thick and sticky in those people who are affectedRead MoreTaking a Look at Cystic Fibrosis1020 Words   |  4 PagesINTRODUCTION Cystic fibrosis (CF) is an inherited autosomal recessive disorder that affects the lungs and digestive system most often. In the United States some 30,000 children and adults have CF. There are approximately 1,000 new cases of cystic fibrosis diagnosed each year in the US with 70% of patients diagnosed with CF by the age of two, 40% of patients with CF are 18 or older. In the 1950s most children with CF did not survive to attend elementary school, but in 2006 the median ageRead MoreTaking a Look at Cystic Fibrosis1094 Words   |  4 PagesCystic fibrosis, an inherited disease of the secretory glands that affects the liver, pancreas, intestines, lungs, sinuses, and sex organs, affects about 30,000 Americans with 1,000 new cases diagnosed each year. Normal mucus is a watery, slick substance made by the tissues that keeps the inside of organs moist, preventing infection. People with cystic fibrosis have thick and sticky mucus that builds up in their lungs, blocking the airways . This buildup can cause serious lung diseases from bacteriaRead MoreA Research Study On Cystic Fibrosis1307 Words   |  6 Pages Brief History Cystic Fibrosis was first recognized in 1938, as an individual disease or distinct entity, which basically means that the symptoms were not related to any other illness (Davis, 2006), but there was a common passage in the ‘Almanac of Children’s Songs and Games from Switzerland’, the passage read, ‘the child will soon die who’s brow tastes salty when kissed’, which hinted at the saltiness of the skin of infants who died might relate to Cystic Fibrosis. Autopsies were done in 1838 onRead MoreCauses And Treatment Of Cystic Fibrosis1549 Words   |  7 Pagesfactor. Carlos is a carrier of Cystic Fibrosis and had a brother who had the disease. Carlos would like Mollie to get test for Cystic Fibrosis before having a child. Mollie is unsure about being tested but agreed to think about it. Cystic Fibrosis affects over 50,000 people in the United States, Canada and Europe (3). One in every twenty Americans are carriers of Cystic Fibrosis, approximately twelve million people are unaware they are carriers (3). Cystic Fibrosis is autosomal recessive inheritedRead MoreGluten, Wheat And Grain Products915 Words   |  4 Pagestests for antibodies specialized to celiac disease. Another test that can be done to diagnose celiac disease is a small intestinal biopsy which uses an EGD (esophagogastroduodenoscopy) to collect samples of the small intestine. Doctors then use this to look for signs of celiac disease. Lactose intolerance is caused by the large intestine’s inability to digest lactose, a type of sugar. When lactose is ingested, an enzyme called lactase in the large intestine works to break down lactose, for people whoRead MoreCystic Fibrosis : A Defect3451 Words   |  14 PagesRunning head: Cystic Fibrosis: A Defect in the CFTR Gene Cystic Fibrosis: A Defect in the CFTR Gene Alexandra L Allen Southern Union State Community College RAD212: Image Evaluation and Pathology Abstract What is Cystic Fibrosis? How does it affect people living with it? Cystic Fibrosis, also known as CF, is a life-threatening hereditary disease. It is inherited by a faulty cystic fibrosis transmembrane conductor (CFTR) geneRead MoreGene Testing : Genes Affect A Single Gene Essay1398 Words   |  6 Pageshereditary unit consisting of DNA that occupies a spot on a chromosome and determines a characteristic in an organism. (Introduction to Genetics, 2016). Genes are passed on from parent to child, which then play an important role in deciphering your child’s looks and behaviour. Unfortunately, some of the genes shared between parents in an offspring are altered in such a way that they create what is called a gene mutation. â€Å"Gene mutations affect a single gene by changing its base sequence, resulting in an incorrectRead MoreCystic Fibrosis Complications And Treatment2289 Words   |  10 PagesCystic Fibrosis Complications and Treatment Cystic Fibrosis (CF) can be hard to perceive because the word does not really describe what the disease really is. When we think of the word Fibrosis, we associate it with a lot of scarring and we relate the word cystic to mean fluid filled sacs. Cystic Fibrosis (CF) is genetic; which means that it comes from our genes and is encoded in our DNA. Our DNA is shaped like a double helix and humans have fourth-six pairs of these in which we get one from eachRead MoreThe Common Genetic Disorders : Cystic Fibrosis2762 Words   |  12 PagesCystic fibrosis is one of the most common genetic disorders. Patients with cystic fibrosis have many serious medical conditions and the majority only live to their mid-thirties. I will be looking at many different aspects of the disease such as, phenotypes, genotypes, and inheritance patterns. Also how the disease is diagnosed, treated, and the prognosis of the disease. According to the American Lung Association, â€Å"Cystic fibrosis is the second most life shortening, inherited disorder occurring