Introduction The genetic autosomal recessive disorder known as Cystic Fibrosis (CF) effects on average 1 of 28 Caucasians. The average age for patients to be diagnosed with this genetic disorder is around 2 weeks and 2 years old, there are some cases where they are find out sooner and others when they are adults. CF affect the patient’s chloride channels which causes the mucus in their lungs to thicken and pool. It can also affect the pancreas by blocking it up and not allowing it to produce digestive enzymes.…
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.…
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,…
Cystic Fibrosis Part 1 Jenna Saline Kaplan University Cystic Fibrosis is a genetic condition that has an affect on many organs of the patient. This disease will ultimately lead to fatal impairment of the lungs. It is most common to see Cystic Fibrosis diagnosed from early childhood to young teens. Cystic Fibrosis is an autosomal recessive disorder in which both gene alleles must be mutated for the disease to be expressed (Ignatavicius and Workman, 2013). As every person is unique, the severity of the effects from CF will vary from person to person.…
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…
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.…
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.…
The anatomical changes that cystic fibrosis has on the endocrine system are poor growth development and delayed puberty in children. This condition affects the pancreas and its secretions. The pancreas is involved with secreting enzymes, that break down food, as well as the hormone insulin, which controls blood sugar levels. Cystic fibrosis causes these secretions to become thicker and pancreatic ducts become blocked.…
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.…
The biological basis and symptoms of Cystic Fibrosis.…
Digestive system complication can be averted with medication with digestive enzymes for the pancreas. Physical therapy can help improve respiratory problems. To prevent infections a person with Cystic Fibrosis should not go near another person with the disease. If a person tells their doctor, their issues the right medication and help can be given and the person can live a healthy…
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.…
Knowing one’s family health history provides families, as well as family health nurses knowledge regarding a patient’s risk for certain diseases (NIH, 2016). As families not only share genes, but their environment, and lifestyle, a family nurse must also consider non-biological factors when completing a family health history (NIH, 2016). The purpose of this paper is to discuss my findings after completing a genetic family history assessment, including three generations, as well as family nursing interventions that may be implemented based on the assessment. Choosing this particular family was based on the knowledge, one member has cystic fibrosis. Family Members and Health History…
The same person may have symptoms that worsen or improve as time passes, and some people may not experience symptoms until adolescence or adulthood. There are many symptoms to cystic fibrosis, some of which can be seen soon after birth. Patients with cystic fibrosis have a higher level of salt inside their sweat, so parents can often taste the salt when they kiss their children. Most other symptoms affect the respiratory system or digestive system, but all U.S. states screen newborns; therefore, if a child has cystic fibrosis, the parent will most likely find out right away. Some of the symptoms that can be experienced later in the process of cystic fibrosis include: coughing up thick mucus, getting sinus infections, bronchitis, or pneumonia often, growths (called polyps) in the nose, bulky, oily, or foul-smelling stool, shortness of breath, too much gas, constipation, or stomach pain, weight loss, or failure to gain weight, low bone density, wide, rounded fingertips and toes “What is Cystic Fibrosis?”.…
Cystic fibrosis (CF) is the genetic disease that affects mostly European. It is one most common autosomal recessive disease in the 1950s. CF is the result of sticky build mucus in the respiratory and digestive system. In the digestive and respiratory system, excessive mucus secretion gets in the way of digestive enzyme and cell membrane of the lung which led to the blockage of absorption of nutrient and exchange of Co2. The symptom of CF is salty-tasting skin, Coughing, Wheezing and bulky stools.…