Cystic fibrosis

and slick and protects the lining of many organs and tissues. Cystic fibrosis causes the body to over produce abnormally sticky and thick mucus, damaging organs and blocking the lungs. It may cause severe breathing issues and create and environment for bacteria to infect the lungs. Cystic fibrosis was discovered in 1938 by Dr. Dorothy Anderson and after more visibility, the disease prompted the creation of the National Cystic Fibrosis Research Foundation in 1955. The disease is genetic,…

Cystic Fibrosis is a disease that is caused by a mutation in the CFTR gene. CFTR stands for cystic fibrosis transmembrane conductance regulator whose mutation commonly leads to the deletion of three nucleotides which code for the amino acid phenylalanine. The mutation, therefore, leads to the loss of this amino acid. The mutant CFTR leads to the disease as the incorrect protein folding is detected in the endoplasmic reticulum which leads the protein to be degraded and thus never reaches the…

Cystic Fibrosis Throughout my examination of the current studies and information of individuals affected by Cystic Fibrosis, I have highlighted the importance of lung transplants needed for these patients especially if this is their only option left. They are given to patients depending on their position on the transplant list but bias remains that the lungs won’t be “put to good use” in Cystic Fibrosis patients. Research indicates that there’s a 67 percent survival rate with lung transplant…

Physiology: In cystic fibrosis the CFTR gene does not produce the chloride pump protein, so water cannot move into the mucus making it very thick and sticky. This abnormally thick mucus builds up in passageways causing obstructions and harboring bacteria that cause infections, especially in the lungs and the pancreas. In the lungs this thick mucus leads to difficulty breathing and because of the bacteria that gets trapped and stuck in the mucus that lines the lungs people with cystic fibrosis…

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…

Cystic Fibrosis is a debilitating, inherited disease which affects the lives of many Americans. There are many symptoms which can be indicative of Cystic Fibrosis. There is no known cure for Cystic Fibrosis, yet there are a variety of treatments. Treatment can assist a victim in managing Cystic Fibrosis and ultimately increase life span. What are the causes, diagnosis process, and treatments for Cystic Fibrosis? Cystic Fibrosis is a life shortening disease which causes an abnormal collection of…

A Matter of Salt- Cystic Fibrosis Dating back from the Middle Ages, European Folklore warned, “woe is the child who tastes salty from a kiss on the brow, for he is cursed, and soon must die”. These children were considered hexed, with death in childhood being common. Though the cause was unknown at the time, this warning referenced children born with cystic fibrosis. Cystic fibrosis is a disease caused by a gene mutation, changing a protein that regulates the movement of salt in and out of…

Article #1 Title: Camps take Cystic Fibrosis Patients Surfing. Posted: Aug 17, 2014 By Krysta Fauria. 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,…

The Cause and Effect of Mutations on the Cystic Fibrosis Transmembrane Conductance Regulator Gene and How it Affects Lung Functions in an Individual Sterling Wood Biology 2458 Section 005, Pankaj B.C., October 11, 2015 Introduction Many people do not realize all the different factors that are a necessity when it comes to just breathing. The air we breathe is filled with many different particles and bacteria that could cause major problems if they were to reach the alveoli. With that being said,…

HS red blood cells have difficulty passing through the spleen, the organ that rids the blood of dead cells and bacteria. Those affected by this condition experience anemia, jaundice, and an enlarged spleen (NLM “Hereditary Spherocytosis”). In Cystic fibrosis, a defective gene causes a buildup of thick, sticky mucus that obstructs the passages of many of the body’s organs. The mucus traps bacteria, which makes the organs susceptible to infection. When mucus is trapped in the lungs, the affected…