Health - Nursing
Cystic fibrosis is a serious disorder that causes severe lung harm and nutritional deficits. An inherited condition, cystic fibrosis affects the cells that manufacture mucus, sweat and digestive juices. Usually, these secretions are thin and slippery, but in cystic fibrosis patients, a defective gene causes the secretions to become thick and sticky. Rather than performing as a lubricant, the secretions stop up tubes, ducts and passageways, particularly in the pancreas and lungs. Cystic fibrosis occurs regularly in white people of northern European ancestry, happening in about one out of three thousand live births. Formerly the majority of people with cystic fibrosis died in their teens. Enhanced screening and treatments currently permit a lot of people with cystic fibrosis to live into their fifties or even longer (Cystic fibrosis, 2011).
A defect in the CFTR gene causes cystic fibrosis. This gene produces a protein that manages the progress of salt and water in and out of the body's cells....
In people who have cystic fibrosis, the gene produces a protein that doesn't work correctly. This leads to thick, sticky mucus and very salty sweat. Research proposes that the CFTR protein also influences the body in other manners. This might assist in explaining other symptoms and difficulties of cystic fibrosis. More than a thousand recognized defects can influence the CFTR gene. What kind of defect a person has may control how severe cystic fibrosis is. Additional genes also might play a role in how harsh the disease is (Cystic Fibrosis, 2011).
The thick and sticky mucus connected with cystic fibrosis blocks the tubes that carry air in and out of a person's lungs. This can cause:
unrelenting cough panting frequent lung infections recurring sinus infections
The thick mucus can also block tubes that transport digestive enzymes from ones pancreas to ones small…
Cystic Fibroids Cystic fibrosis Cystic fibrosis is a disease that can be passed down from one generation to the other. It affects secretary glands that produce mucus and sweat. The disease results after the fibrosis transmembrane conductance regulator (CFTR) gene that is found on chromosome 7 has undergone some sort of mutation. Mutation on chromosome 7 alters the production and function of CFTR glycoprotein (Scott, 2013). Studies have identified more than 1600
Cystic Fibrosis (CF) is genetically inherited through a defective gene, which results in the body producing "abnormally thick and sticky fluid, called mucus. This mucus builds up in the breathing passages of the lungs and in the pancreas, the organ that helps to break down and absorb food." (PubMed Health, 2011) Reports state that millions of Americans carry the defective Cystic Fibrosis gene however; most do not have any symptoms since
Cystic Fibrosis: The Facts is a comprehensive, informative, and well-written book about the disease and its treatments. Ann Harris and Maurice Super address the book to a general audience, making the book extremely accessible to laypeople. Cystic Fibrosis: The Facts is an ideal source for people suffering from cystic fibrosis or for people who have loved ones suffering from the disease. Harris and Super divide the 129-page book into several
" (Karem et al., 1073) With an increased focus today on the genetic implications of the condition, enhanced abilities to understand the behaviors of human DNA are opening the door to a more perceptive response to the condition in question. As the text by Davis (1993) indicates, "as mutational analysis and patient data continue to be compiled, patient genotyping should prove useful in both prognosticating and providing a framework for evaluating
Cff.org/will each be the source of information and professional peer reviewed articles will be cited from these sources and identified by source as they cited. There is a wealth of available information, data and studies on CF. What it all means to the patients who suffer from this debilitating and life-threatening disease will be understood as this essay proceeds. Chapter One Diagnosis and the Anatomy and Physiology of a Life Threatening Disease: Cystic
However, treatments can be used to reduce, if not nearly completely diminish, symptoms and minimize any other complications. Here are the conditional means: Therapy: People with cystic fibrosis need a way to physically remove thick mucus from their lungs. This is often done by manually clapping with cupped hands on the front and back of the chest -- a procedure that's best performed with the person's head over the edge of