Cystic fibrosis

Cystic fibrosis (CF) is a chronic disease that imitates organs such as the liver, lungs, pancreas, and intestine. It interrupts the body’s salt balance, separating little salt and water on the exterior of cells and affecting the thin layer of the mucus that normally keeps the lungs free of germs to become dense and tacky. This mucus is tough to cough out, and it chokes the lungs and airways, leading to infections and injured lungs. It is also known as mucuviscidosis because of the mucus that constructs

from dehydrating. A normal people wouldn’t have a problem inhaling Cystic Fibrosis is inherited disease The disease starts because the 7th chromosome that makes a protein called Cystic Fibrosis Transmembrane Regulator or CFTR has mutated and now the body produces to much of the protein Sweat glands Cystic Fibrosis causes the body to release more salt in sweat which causes problems when exercising. Reproductive System Cystic Fibrosis can causes the person to become infertile in about 90% of men and

Patient, The testing of your child's screening has come back. I am sorry to inform you that your child is suffering from Cystic Fibrosis according to the sweat test. Although your child has this, it is at an early stage and can be treated. Cystic fibrosis is a defect (mutation) in a gene that changes a protein that regulates the movement of salt in and out of cells (Cystic Fibrosis, October 2016). Your child may suffer from some symptoms like thick, sticky mucus in the respiratory, digestive and reproductive

Nicole Davis EDU 222 Professor Hanson 12/5/16 Cystic Fibrosis Cystic Fibrosis, otherwise known as CF, is an inherited genetic disease that affects the lungs and digestive system. The disease causes a build-up of thick mucus in the lungs and other organs. Mucus clogs the airways in the lungs and “traps bacteria, leading to infections, extensive lung damage, and eventually, respiratory failure. In the pancreas, the mucus prevents the release of digestive enzymes that allow the body to break down food

Manuel Alberto Tello Garibay Biology 181 Tuesday/Thursday Cystic Fibrosis Cystic Fibrosis (CF) is a disorder that is passed down from parent to child, which primarily occurs in the Secretory gland, this is the part of the human body that produces mucus. This by all mean does not indicate that the parents are affected, but instead states that they are carriers of this disorder. This is the reason why CF is said to be a recessive trait as oppose to a dominant trait. The main affected

What is it? : Cystic Fibrosis is a genetic life threatening disease that causes severe damage to the lungs and digestive system and slowly limits your breathing. What happens with CF is there is a large buildup of mucus in the lungs, pancreas, liver, intestines, sinuses, and sex organs. The mucus is usually made of sweat and digestive juices that are meant to act as lubricant but end up clogging up and blocking tubes, ducts and passageways. With the buildup of mucus it makes it easier for certain

small town of Kosciusko, Mississippi, was diagnosed with cystic fibrosis when she was only six months old. Cystic Fibrosis, (CF) is an inherited life-threatening disorder that damages the lungs and digestive system. Mucus builds up in the lungs and blocks the person’s airway, causing this person to have trouble breathing regularly. CF is a genetic disease, meaning that a person does not catch it, it is passed down through DNA. Cystic Fibrosis last with a person his or her entire life time. It occurs

baby’s symptoms, I believe that the first differential diagnosis would be Cystic Fibrosis (CF). She has the classic symptoms of Cystic Fibrosis which are foul- smelling, fatty diarrhea. According to the National Organization for Rare Disorders ([NORD] 2016), cystic fibrosis is a genetic disorder which affects multiple organs in the body. Cystic fibrosis is inherited and is caused by the mutations in the cystic fibrosis gene, transmembrane conductance regular. The abnormalities affect certain glands

Cystic Fibrosis (CF) is an autosomal recessive genetic disease that causes thickened mucus to form in the lungs, pancreas, and other organs. It affects a specific protein called Cystic Fibrosis Transmembrane Regulator (CFTR) that controls the normal movement of sodium, chloride, and water in and out of the cells within the body. Those diagnosed with CF have either too little or abnormal CFTR. When CFTR is absent or defective, the mucus usually secreted by the cells in the pulmonary airways, pancreatic

Cystic fibrosis is a debilitating, genetic, disease that affects the mucus glands of the lungs, pancreas, and other organs. To fully comprehend the everyday affects, envision Emily, a fourteen-year-old girl struggling to adapt to high school life with cystic fibrosis. She spends over three hours a day solely nebulizing and performing airway clearance therapy; this time does not include doctor’s visits or other therapists’ appointment (Sawicki, 2008). Due to the high treatment demand, Emily feels