"Cystic Fibrosis" Essays and Research Papers

Cystic Fibrosis

Cystic fibrosis is when thick mucus is produced due to a hereditary genetic disorder; the mucus produced is so thick that it clogs the body’s tubes and passageways. Cystic fibrosis is caused by the mutation in a gene known as the CFTR gene; this fault in the gene causes the normal workings of a protein to be blocked allowing too much salt and not enough water into cells. These result in the build-up of thick mucus in the body’s tubes and passageways blocking them, these blockages damage the lungs...

Premium Asthma, Bronchitis, Cystic fibrosis 1285  Words | 4  Pages

Open Document

Cystic Fibrosis

A Nursing Diagnosis for Cystic Fibrosis Nursing diagnoses describe problems that can be addressed by nursing measures. Because nurses can't diagnose a disease or prescribe medication, a nursing diagnosis doesn't describe a disease or prescribe medications or treatments beyond a nurse's scope of practice. In the case of a disease like cystic fibrosis, nursing diagnoses center on treating problems caused by the disease. Description According to the North American Nursing Diagnosis Association, or...

Premium Bacteria, Cystic fibrosis, Lung 1018  Words | 4  Pages

Open Document

Cystic Fibrosis

Very, VERY unlucky. I just so happen to be closely related to one of these “unlucky” individuals. No, he’s not unlucky because he’s married to my sister (which I’m sure pains him on some occasion, anyway) but rather because he was born with Cystic Fibrosis, or CF, to those of us “in the know”… So what is CF? Other than being a painful, inconvenient, soul-sucking bitch (female dog) of a hand to be dealt, it’s a chronic disease affecting multiple organs and systems of the body. It IS genetic...

Premium Amniocentesis, Asthma, Chorionic villus sampling 1221  Words | 4  Pages

Open Document

Cystic Fibrosis Research Paper

Cystic Fibrosis Cystic Fibrosis, a very serious inherited genetic disease, is also known as CF and sixty-five roses. This disease affects one in every 3,000 live births. It may first appear in a newborn, but can appear all the way up until a young adult. However, ten percent of most cases are apparent at birth. CF affects the lungs and causes a build-up of abnormally thick mucus which leads to chest infections, and CF also affects the reproductive system. Doctors do not know what causes the mucus...

Premium Asthma, Cystic fibrosis, Digestion 990  Words | 3  Pages

Open Document

Cystic Fibrosis

ASSIGNMENT TITLE: ESSAY ASSIGNMENT SUBTITLE: CYSTIC FIBROSIS COURSE CODE: BIOL 172 COURSE TITLE: STRUCTURE AND FUNCTION OF THE HUMAN BODY II CRN: 12495 SEMESTER: STUDENT NAME: STUDENT ID: PROGRAMME: BSC GENERAL NURSING DATE OF SUBMISSION: 27-11-2012 LECTURER’S NAME: JO ELLEN COLE Cystic fibrosis is an inherited gene caused by a defective gene, which affects tissues that produce mucous secretions. Cystic fibrosis affects organs like the lungs, the gastrointestinal...

Premium Cystic fibrosis, Cystic fibrosis transmembrane conductance regulator, Digestion 2295  Words | 7  Pages

Open Document

Cystic fibrosis

Speech Outline *Title: Cystic Fibrosis *Specific Purpose: To inform my classmates about cystic fibrosis and how severe it really is. *Thesis Statement: Cystic Fibrosis is a disease that is slowly killing our children and the question is how can we help these children in their times of need? Introduction Attention-getter: How many people love children? how would you feel if you knew that a mass majority of our youth has been born with and/or died from cystic fibrosis? Preview: Today I will be...

Premium Cancer, Cystic fibrosis, Cystic Fibrosis Foundation 887  Words | 3  Pages

Open Document

Cystic Fibrosis and Asthma

There is an estimated 30,000 people in the United States that have Cystic Fibrosis (CF) and about 25 million who have asthma. CF is often confused with asthma because of their symptom similarities. CF, despite what people may think is far more severe than asthma. Most people think that CF would be easier to treat and cure because there are fewer people with it. Unfortunately, at this point there is no cure for CF. Cystic Fibrosis is far more severe than asthma because it is terminal, the treatment...

Premium Asthma, Bacteria, Cystic fibrosis 1094  Words | 3  Pages

Open Document

Explain Cystic Fibrosis

Cystic Fibrosis- ELT 2 The Problem Section One Cystic Fibrosis, also known as mucovoidosis, or mucoviscidosis, is an incurable, inherited genetic condition caused by two homozygous recessive alleles. In order for a child to inherit this disorder, both of its parents must either be a sufferer or carrier of the gene. The condition itself is caused by a faulty gene found on chromosome seven that controls the movement of salt and water through the cell membrane.  In cases of Cystic Fibrosis...

Premium Asthma, Bronchitis, Cystic fibrosis 975  Words | 4  Pages

Open Document

CYSTIC FIBROSIS

Cystic fibrosis is a chronic lung disorder caused by an autosomal recessive multiorgan disorder. The disorder is due to an exocrine gland dysfunction. The deficiency in chloride flow and increase sodium absorption results in thick sticky mucous that clogs the lungs and obstruct glands The pancreas obstruction leads to the failure of secretion of enzymes. The chronic lung disorder is prevalent amongst Caucasians. “Cystic fibrosis occurs in one of 2,5000Caucasians,approximately 30,000 individuals...

Premium Asthma, Chorionic villus sampling, Cystic fibrosis 1488  Words | 5  Pages

Open Document

Cystic Fibrosis Case Study

Krickett Davis Zachary Mock Cystic Fibrosis Case Study: Part I Questions: The Meeting Consult your textbook and trustworthy Internet sites to answer the following questions: 1. Which organs are affected by cystic fibrosis? What are the disease symptoms? Organs that are affected by cystic fibrosis include the lungs, pancreas, liver, sweat glands, reproductive organs, nose and sinuses. The symptoms of cystic fibrosis include coughing with mucus coming up, wheezing, breathlessness, decrease in ability...

Premium Allele, Amino acid, Cystic fibrosis 1424  Words | 5  Pages

Open Document

Cystic Fibrosis Case Study

Christopher Smith Miss Chiu AP Bio CF Case Study March 19, 2015 Questions: 1. Currently, scientists believe that Cystic Fibrosis is caused by a defect in the CFTR gene causes cystic fibrosis (CF). This gene makes a protein that controls the movement of salt and water in and out of your body's cells. In people who have CF, the gene makes a protein that doesn't work well. This causes thick, sticky mucus and very salty sweat. Every person inherits two CFTR genes—one from each parent. Children...

Premium Asthma, Cell, Cystic fibrosis 857  Words | 5  Pages

Open Document

Cystic Fibrosis

Cystic Fibrosis Julie LeBeau Mildred-Elley BIO 210 February 20, 2014 Cystic Fibrosis Cystic Fibrosis is a fatal genetic disorder that effect’s many organ systems in the body. It is estimated that CF effects 30,000 adults and children in the United States, with approximately 1,000 new cases diagnosed each year. Cystic Fibrosis is most prevalent among white but affects all ethnic groups. Cystic Fibrosis results from an autosomal recessive gene mutation of the Cystic Fibrosis transmembrane...

Premium Allele, Asthma, Cystic fibrosis 936  Words | 3  Pages

Open Document

Stem Cells and Cystic Fibrosis

Stem cells – the cure to Cystic Fibrosis? Cystic Fibrosis is one of the UK's most common life threatening diseases with it affecting over 9,000 people. Statistics show that one in twenty five people in the UK carry the faulty gene, each week five babies are born with the disease and another two young lives are lost. Cystic Fibrosis is a genetic disorder caused by a recessive allele. It affects the internal organs, especially the lungs and digestive system, by clogging them with thick sticky mucus...

Premium Bone marrow, Cell, Cell division 810  Words | 3  Pages

Open Document

Cystic fibrosis, PKU and the Digestive system

Cystic fibrosis, PKU and the Digestive system 1. What are the symptoms of cystic fibrosis and PKU with respect to the digestive system? Symptoms for cystic fibrosis include diarrhea that does not go away, foul-smelling stools, greasy stools, frequent urinating, frequent episodes of Pneumonia, persistent cough, skin tastes like salt, poor growth, chronic sinus infection. When phenylalanine builds up it affects brain functions and the central nervous system. Some symptoms include: skin problems...

Premium Cystic fibrosis, Digestion, Mental retardation 923  Words | 4  Pages

Open Document

Cystic Fibrosis

Cystic fibrosis: Overview and Implications Christopher Phillips, SN BTC Blackhawk Technical College Health Promotion 02/14/13 Cystic Fibrosis: Overview and Implications Cystic fibrosis (CF) is a worldwide autosomal recessive disorder genetically inherited that causes chronic progressive health alterations of the bodily systems (Lyczak et al, 2004, p. 194). Mutations in the cystic fibrosis transmembrane conductance regulator gene (CFTR), located on the long arm of chromosome seven, results...

Premium Cystic fibrosis, Cystic fibrosis transmembrane conductance regulator, Life expectancy 1756  Words | 5  Pages

Open Document

Treatments for Lung Conditions in Cystic Fibrosis Sufferers

FOCUS: “Treatments for lung conditions Cystic Fibrosis sufferers contend with” Word Count: 1461 This essay will aim to explore the different ideas and concepts of using several types of medication for cystic fibrosis sufferers. Cystic fibrosis is a genetic disorder that affects thousands of children and adults across the United Kingdom; it mainly affects Caucasian beings and is a well-known disease throughout the world, but has no cure only treatments to ensure a better quality of life...

Premium Case study, Cystic fibrosis, Lung 1486  Words | 4  Pages

Open Document

Cystic Fibrosis Research Paper

Cystic Fibrosis- Option 2 Justin Jang and Junior Suwannapeng Jasper High School Cystic fibrosis is an autosomal (not sex linked), hereditary disease caused by a mutation in the gene called the cystic fibrosis transmembrane conductance regulator gene, or the CFTR gene. This CFTR gene belongs to a group of genes called ABC (ATP-binding cassette). These are transport molecules for molecules such as phosphate, glucose, chloride, and peptides. Specifically for the CFTR gene, the molecules transported...

Premium Amino acid, Bacteria, Cell membrane 1736  Words | 5  Pages

Open Document

Cystic Fibrosis

Cystic Fibrosis Cystic Fibrosis (CF) is the most common life-threatening genetic disease and is a progressive, permanent disorder in which the glands making sweat, mucus and intestinal secretions don’t function correctly. Clinical Symptoms The accumulation of thick, sticky mucus associated with CF, blocks the tubes that transport air resulting in lung and sinus infections, wheezing and persistent coughs. Thick mucus can obstruct tubes that transport digestive enzymes from the pancreas to the...

Free Cell, Cystic fibrosis, DNA 386  Words | 2  Pages

Open Document

Eman

cause life time diseases. Cystic fibrosis is a disease caused by a frame shift mutation. Frame shift mutations are unhealthy because it causes diseases, there is no cure, and it can be passed down to new born babies. Cystic fibrosis is a caused by a frame shift mutation specifically, deletion mutation. Cystic fibrosis is an inherited chronic disease that affects the lungs and digestive system. Peter Crosta says, “Cystic fibrosis occurs in the gene called cystic fibrosis transmembrane conductance...

Premium Cystic fibrosis, Digestion, Digestive enzyme 1277  Words | 3  Pages

Open Document

Genetics and Unaffected Female Generation

the images below and answer the follow-up questions. Questions: 1. According to the pedigree, is cystic fibrosis inherited as a dominant or as a recessive trait? Explain how you made your conclusion using evidence from the pedigree and the principles of genetics. Cystic fibrosis is a recessive trait. If you have one CF gene and one non-CF gene, you will be a carrier but not have CF. I referred back to Mendel mentioning that the trait...

Premium Allele, Bacteria, Biology 418  Words | 4  Pages

Open Document

Life Factors and Life Events

a person’s life are cystic fibrosis, celiac disease, asthma, brittle bone disease and rheumatic disease the genetic disease that I have chosen to write about is cystic fibrosis. Cystic fibrosis Cystic fibrosis is an inherited disease that is caused by a defective gene; cystic fibrosis affects the glands in the body that produce our bodily fluids. Cystic fibrosis is not very common in the UK as only 4% of the population are thought to be carrying this gene. The cystic fibrosis gene is a recessive...

Premium Affect, Affect display, Cystic fibrosis 2585  Words | 6  Pages

Open Document

Unit Project 4

A Typical Cold? by Brent J.F. Hill Part III—Your Explanation of Sam’s Condition Objectives and Issues 1. What type of disease is Sam suffering from? Cystic Fibrosis 2. What tissues and organs does this disease affect? Once you identify all the tissues and organs, briefly explain their respective dysfunction. Exocrine Glands – glands may become blocked, produce excessive secretions Sweat Glands – extreme decrease in salt reabsorbtion, resulting in high salt content in sweat. Lungs – Mucus...

Premium Asthma, Cystic fibrosis, Exocrine gland 1226  Words | 4  Pages

Open Document

Cystic Fibrosis

8-27-13 Genetics Cystic Fibrosis Cystic Fibrosis is one of the most widespread genetic disorders in the modern world. While only 30,000 members of the American population is affected by the disease, millions of Americans are carriers of the disease; the difference between carriers and sufferers of the disease lies in the autosomal recessive nature of Cystic fibrosis. A truly documented history of Cystic fibrosis did not exist until well into the 1930s, although people did have an idea of...

Premium Chromosome, Cystic fibrosis, DNA 363  Words | 2  Pages

Open Document

Commemorative Speech

has Cystic Fibrosis. But she is so much more than that. She is my personal hero and I could not imagine my life without her. Today I want to share some of the qualities that make her so important to me. Today I will tell you about my limitless, lovable, and loyal Lisa. Low to that child which kissed on the forehead tastes salty, he is bewitched and will soon die. This folklore handed down through the ages is an early description of the disease now known as Cystic Fibrosis. Cystic Fibrosis is an...

Premium Breathing, Cystic fibrosis, Expiration 975  Words | 3  Pages

Open Document

A Typical Cold

” please check with the instructor. Your next task is to prepare a group report that addresses the points detailed below. Objectives and Issues to Address in Preparing Your Final Group Report 1. What type of disease is Sam suffering from? Cystic fibrosis 2. What tissues and organs does this disease affect? Once you identify all the tissues and organs, briefly explain their respective dysfunction. It affects the lungs, liver, gallbladder, intestines, sweat glands, reproductive organs, and the...

Premium Anemia, Asthma, Blood 2183  Words | 7  Pages

Open Document

cystic fibrosis

Cystic Fibrosis is a disease that causes mucus like substance to accumulate in the lungs, digestion track and various parts of the body. This is a disorder of the exocrine glands. Cystic Fibrosis is most common in children and young adults. This disease is usually not found in people over the age of forty years old because you are born with the disease and normally die young. This is a very harsh disease that makes it extremely hard to breathe. There are over one-thousand people diagnosed with...

Premium Chromosome, Cystic fibrosis, Mucus 621  Words | 2  Pages

Open Document

cystic fibrosis

large amounts of body salt when they sweat on hot days. Cystic fibrosis is the most common cause of pancreatic insufficiency in children, but a condition called Shwachman-Diamond Syndrome (SDS) is the second most common cause. SDS is a genetic condition that causes a reduced ability to digest food because digestive enzymes don't work properly. Some of the symptoms of SDS are similar to those of CF, so it may be confused with cystic fibrosis. However, in kids with SDS, the sweat test is normal. ...

Premium Asthma, Bacteria, Cystic fibrosis 624  Words | 2  Pages

Open Document

NRS 434V Group PP Week 4 1

CYSTIC FIBROSIS Lori Alley Erika Lemerande Nicole Carpenter Maureen Joseph June Reyes Clinical Description and Definition of the Disease. “Cystic Fibrosis is a life threatening, genetic disease that causes persistent lung infections, and progressively limits the ability to breathe” (“Cystic Fibrosis,” n.d.). Pathophysiology and History of the Disease • Cystic Fibrosis is caused by defects in the cystic fibrosis gene. • Cystic Fibrosis was recognized over 400 years ago in Germany. • There is no...

Premium Cystic fibrosis, Health care 824  Words | 19  Pages

Open Document

Effects of Factors

Potential effects of different factors on development I am going to write about the following factors and how they may affect the development of an individual. · Rubella (Biological) · Cystic fibrosis (Genetic) · Smoking (Lifestyle) · Poor Housing (environmental) · Poverty (Socio-economic) Rubella & CRS Rubella is an infection also known as German measles. It is most common amongst children but may also affect adults. It is passed on through the tiny droplets in the air. If a pregnant woman...

Premium Affect, Congenital rubella syndrome, Cystic fibrosis 1639  Words | 4  Pages

Open Document

FlowersAylaInheritedDiseaseUnit7

I realized that one serious disease that I have a chance of developing at some point in my life is Cystic fibrosis. Many people are familiar with cystic fibrosis or have heard about it at some point in time in their life. According to an article that I read Cystic fibrosis is a buildup of thick, sticky mucus that can damage many of the body’s organs (“Genetic Home Reference”, 2012). Cystic fibrosis is a genetic disease, and it is inherited by autosomal recessive, which means that there must be two...

Premium Cancer, Cystic fibrosis, Disease 960  Words | 5  Pages

Open Document

Genetically Designing Children

The survey found that 56% supported using them to counter blindness and 75% for mental retardation” (Naik 2). One example of a disease that can be prevented is cystic fibrosis. In vitro fertilization and diagnosis during embryonic development basically only allows the unaffected embryos to be chosen for transfer into the uterus. Cystic fibrosis is a debilitating disease that affects the lungs and digestive system. It is caused by a defective gene and its protein product (CFF 1). People that have this...

Premium Cystic fibrosis, Genetics, Huntington's disease 1810  Words | 5  Pages

Open Document

Cchmc Case

efficacy—for example, implementing a "forcing function" into the operating room process that keeps patients out of the OR until they've received antibiotics, thus reducing surgical site infections. For another project, she selects the hospital's Cystic Fibrosis (CF) Clinic, in part because its head physician was the only division leader who showed any interest in participating in improvement initiatives. These factors along with the change in the vision and new leadership triggered the initiation of...

Premium Better, Cystic fibrosis, Doctor-patient relationship 1242  Words | 4  Pages

Open Document

Comparative Literature

Topic: Cystic Fibrosis Introduction Cystic Fibrosis (CF) according to Cohen 2004, is the most common fatal hereditary disease amongst children and adults. It is an autosomal recessive disorder, and most carriers of the gene are asymptomatic. The flawed gene that causes CF affects the glandular secretions by altering chloride transport across cell membranes. Thickening of bronchial secretions leads to infection and other respiratory disorders. Other mucus secreting glands...

Premium Asthma, Cystic fibrosis, Digestion 2336  Words | 7  Pages

Open Document

Cystic Fibrosis

1. Describe the symptoms of cystic fibrosis. The different symptoms of cystic fibrosis include repeated infections and thick mucus secretions in the lungs, it affects you with wheezing, a chronic cough, bronchitis, asthma, weight loss, dehydration, and many more mainly affecting the lungs and stomach. Sufferers may also feel very fatigued easily. 2. Describe two problems associated with the presence of thick, sticky mucus (a) in the lungs and breathing passageways (b) in the digestive system ...

Premium Asthma, Bronchitis, Cystic fibrosis 278  Words | 2  Pages

Open Document

Life Factors

an individual. Genetic factors Cystic fibrosis is caused by a flawed gene. Children will only develop cystic fibrosis if both parents are carriers of the gene. Its protein product causes the lungs to become sticky and clogged. People with cystic fibrosis tend to suffer from chest and respiratory infections which is life threatening as it affects their breathing and they will also have problems absorbing food. Physical development-children with cystic fibrosis tend to go through puberty 2 or 3...

Premium Abuse, Bullying, Cystic fibrosis 1339  Words | 4  Pages

Open Document

Interference with gas exchange

severe, the affected person is generally admitted to hospital. Cystic fibrosis (CF), also known as mucoviscidosis, is an autosomal recessive genetic disorder that affects most critically the lungs, and also the pancreas, liver, and intestine. It is characterized by abnormal transport of chloride and sodium across an epithelium, leading to thick, viscous secretions.[1] The name cystic fibrosis refers to the characteristic scarring (fibrosis) and cyst formation within the pancreas, first recognized in...

Premium Asthma, Chronic obstructive pulmonary disease, Cystic fibrosis 955  Words | 3  Pages

Open Document

A Typical Cold? by Brent J.F. Hill

” please check with the instructor. Your next task is to prepare a group report that addresses the points detailed below. Objectives and Issues to Address in Preparing Your Final Group Report 1. What type of disease is Sam suffering from? Cystic Fibrosis 2. What tissues and organs does this disease affect? Once you identify all the tissues and organs, briefly explain their respective dysfunction. Exocrine glands: Obstructed by viscid or solid materials in the lumen, produce excess secretions...

Premium Anemia, Asthma, Blood 1483  Words | 5  Pages

Open Document

P2 - Effects of five life factors on individual development

P2 – Effects of five life factors on individual development Genetic factors such as cystic fibrosis for example, are life factors which can affect the development of an individual. It can affect an individual at any age and is caused by a faulty gene that is passed from the parents to the child. The faulty gene allows too much salt and not enough water into cells and makes a build up of thick, sticky mucus in the body’s tubes. This can cause blockages in the body’s tubes and passageways, and causes...

Premium Affect, Asthma, Cystic fibrosis 2267  Words | 6  Pages

Open Document

Lung transplant

quality of their life. (Bonser, et al, 2012) Lung transplants are commonly recommended for patients under the age of 65 who have been diagnosed with severe types of lung and diseases such as cystic fibrosis, chronic obstructive pulmonary disease (COPD), interstitial lung disease, idiopathic pulmonary fibrosis or pulmonary hypertension. The procedure is not commonly considered for mild cases, but for those who have exhausted all other options and are likely to die without the transplant. Contraindications...

Premium Chronic obstructive pulmonary disease, Cystic fibrosis, Heart 1741  Words | 5  Pages

Open Document

Cystic Fibrosis Paper

Cystic Fibrosis Cystic Fibrosis is caused by a single faulty gene that controls the movement of salt in the body. In people with Cystic Fibrosis, the internal organs become clogged with thick, sticky mucus resulting in infections and inflammation making it hard to breathe and digest food. For a baby to be born with Cystic Fibrosis, both parents must be carriers of the faulty CF gene. The diagram shows how CF is inherited. Where both parents carry the faulty gene, each child has a one in four chance...

Premium Cirrhosis, Cystic fibrosis, Digestion 506  Words | 2  Pages

Open Document

Cystic Fibrosis: A Genetic Disorder

CYSTIC FIBROSIS ONE OUT OF EVERY 2,500 BIRTHS IN THE UNITED STATES WILL BE DIAGNOSED WITH CYSTIC FIBROSIS. THIS FACT MAKES CYSTIC FIBROSIS ONE OF THE MOST COMMON GENETIC DISEASES IN THE NATION. ABOUT 30,000 AMERICANS HAVE THE DISEASE, BUT EVEN THOUGH CYSTIC FIBROSIS IS THE NATIONS MOST COMMON GENETIC DISEASE THE MAJORITY OF AMERICANS KNOW LITTLE ABOUT IT. CYSTIC FIBROSIS IS RELATIVELY COMMON IN CALCASTION PEOPLE BUT RARE IN AFRICAN-AMERICAN. THE DISEASE IS VERY UNCOMMON IN MONGOLIANS. FIVE...

Premium Bacteria, Cell, Cystic fibrosis 510  Words | 2  Pages

Open Document

Spontaneous Pneumothorax

People who dive or participate in high altitude flying can also have primary SP because of the changes in altitude (Merck, 2005). A secondary SP occurs in people with extensive lung damage. Many types of lung diseases such as COPD, emphysema, cystic fibrosis, sarcoidosis, TB, and pneumonia can cause a secondary SP (Merck, 2005). A secondary SP is much more life threatening because the person already has decreased lung function and the SP only decreases it more. A catamenial SP is a very rare condition...

Premium Cystic fibrosis, Lung, Merck Manual of Diagnosis and Therapy 1357  Words | 4  Pages

Open Document

Cystic Fibrosis: An Overview

------------------------------------------------- Introduction Cystic fibrosis (also called CF or mucoviscidosis) is an autosomal recessive genetic disorder that affects most critically the lungs, and also the pancreas, liver, and intestine. It is characterized by abnormal transport of chloride and sodium across an epithelium, leading to thick, viscous secretions. The name refers to the characteristic scarring (fibrosis) and cyst formation within the pancreas that was first recognized in the...

Premium Bacteria, Cystic fibrosis, Genetic disorder 6656  Words | 19  Pages

Open Document

Collins Notes

there are multiple genetic risk factors that contribute to these conditions disease = polygenic: power of each individual genetic risk factor low, illness usually develops with combination of several along with appropriate environmental stimuli Cystic Fibrosis: deletion of 3 letters out of 3 billion results in multi-organ disease that affects ~3,000 individuals of northern European background other genes in genome can serve as “modifiers” most genes have some degree of normal variation, normal variation...

Premium Cancer, Chromosome, Cystic fibrosis 949  Words | 3  Pages

Open Document

Science and My Daily Life

chances are 5:30am would not be the time I would be getting up. I then go upstairs and wake up my sons Warren and Ryely to get ready for school. When Warren comes down stairs I help him get his morning treatment machines ready. Warren was born with Cystic Fibrosis and relies on science and the continuing scientific advances of treatments, medicines and therapies to continue living. Warren’s first treatment is called a nebulizer, this lasts about 15 minutes. The nebulizer loosens the thick mucus on the walls...

Premium Circuit breaker, Cystic fibrosis, Incandescent light bulb 1834  Words | 4  Pages

Open Document

NUR/427 personal impact paper

 Cystic Fibrosis: A Personal Impact Carrie Minton NUR/427 June 8th, 2013 Dr. Angela Lowery Cystic Fibrosis: A Personal Impact Isabel and Anabel Stenzel, identical twins, were born with the deadly chronic disease, Cystic Fibrosis. This disease has had a huge impact on their everyday quality of life as well as their family and friends. It is a daily fight and struggle. Not giving up and continuing to be proactive about caring for themselves is key to survival. At birth the doctor...

Premium Asthma, Chronic obstructive pulmonary disease, Cystic fibrosis 1459  Words | 5  Pages

Open Document

Cystic Fibrosis Treatment

Cystic Fibrosis What is Cystic Fibrosis? Cystic fibrosis is a disease passed down through families that causes thick, sticky mucus to build up in the lungs, digestive tract, and other areas of the body. It is one of the most common chronic lung diseases in children and young adults. It is a life-threatening disorder. Causes It is a disorder that occurs due to mutation in the Cystic Fibrosis Transmembrane Conductance Regulator {CFTCR} gene. This gene codes for a product that influences the production...

Premium Asthma, Bronchitis, Cystic fibrosis 565  Words | 2  Pages

Open Document

Nature Nurture Debate

as it occurs throughout all races no matter what their surrounding environment is like. Cystic Fibrosis is a genetic disorder that affects the lungs, pancreas, liver and intestines. Cystic Fibrosis is caused by a mutation in the gene for protein. Cystic Fibrosis is common in a lot of race and gender and is not determined by the surrounding environment as it is caused when the neither of the CFTR (cystic fibrosis transmembrane conductance regulator) gene is working as a result of mutation and therefore...

Premium Biological determinism, Cystic fibrosis, Cystic fibrosis transmembrane conductance regulator 958  Words | 3  Pages

Open Document

History of Cystic Fibrosis

History of Cystic Fibrosis “Woe to that child which when kissed on the forehead tastes salty. He is bewitched and soon must die.” This proverb, dating back to European folklore in the 1700’s, was the diagnosis for the disease recognized today as Cystic Fibrosis (CF). In that time period the disease was usually fatal and common among infants. The excessive salt in the sweat, just one symptom of CF, made the disease identifiable. However, since the time of European folklore, various renowned scientists...

Premium 1950s, Cystic fibrosis, Cystic fibrosis transmembrane conductance regulator 708  Words | 2  Pages

Open Document

Case Study

The symptoms that are associated with cystic fibrosis can be reduced through diet and exercise, support can be provided from staff at specialist centre for cystic fibrosis. There are many support clinics available for individuals that suffer from cystic fibrosis. These clinics tend to be separated between those for children and those for adults. Children that suffer from cystic fibrosis can normally receive care in a general hospital if there is a cystic fibrosis clinic present. As well as the individual...

Premium Cystic fibrosis, Emotion, Grief 482  Words | 2  Pages

Open Document

life stages

free from alcohol-related defects and have a chance for a healthy life. Cystic fibrosis Cystic fibrosis is a serious inherited disease which mainly affects the lungs and pancreas, but can involve other organs including the liver, reproductive organs, nose and sinuses and also sweat glands. Normally cells in these parts of the body make mucus and other watery juices and secretions. In people with cystic fibrosis, these cells do not function correctly and make mucus and secretions which are...

Premium Alcohol, Alcohol abuse, Asthma 2202  Words | 5  Pages

Open Document

Unit 4- Life Factors

organisms. Cystic Fibrosis Cystic Fibrosis (CF) is one of the UK's most common life-threatening inherited diseases. It is caused by a faulty gene that controls the movement of salt and water in and out of the cells within the body. Cystic Fibrosis affects the internal organs, especially the lungs and digestive system, by clogging them with thick sticky mucus. This makes it hard to breathe and digest food. If two carriers have a child, the baby has a 1 in 4 chance of having Cystic Fibrosis. Each week...

Premium Air pollution, Anxiety, Cystic fibrosis 3141  Words | 9  Pages

Open Document

Work

Genetic Counselor Virginia Beach Genetics Counseling Service * Cystic fibrosis is a life-threatening disorder that causes severe damage to the lungs and digestive system. An inherited condition, cystic fibrosis affects the cells that produce mucus, sweat and digestive juices. These secreted fluids are normally thin and slippery. But in cystic fibrosis, a defective gene causes the secretions to become thick and sticky. Cystic fibrosis signs and symptoms vary, depending on the severity of the disease...

Premium Asthma, Bronchitis, Cystic fibrosis 394  Words | 2  Pages

Open Document

Ion Channel Disease

characterized the genes encoding many of these proteins. Ion-channel proteins are under intense scrutiny in an effort to determine their roles in pathophysiology and as potential targets for drugs. Defective ion-channel proteins are responsible for cystic fibrosis,1 the long-QT syndrome,2 heritable hypertension (Liddle’s syndrome),3,4 familial persistent hyperinsulinemic hypoglycemia of infancy,5,6 hereditary nephrolithiasis (Dent’s disease), and a variety of hereditary myopathies,7-9 including generalized...

Premium Action potential, Cystic fibrosis, Electrophysiology 8085  Words | 31  Pages

Open Document

Watson's Theory of Human Caring

relationship (Falk Rafael, 2006). Caring moment I had a caring moment with a Mother of the patient in the NICU that I was caring for. This baby had been admitted with an intestinal obstruction and they had told the parents that they thought she had Cystic Fibrosis. The baby’s mom would come to the NICU everyday and sit with her baby. She was unable to hold the baby as the baby was still critically ill. The baby was intubated and was on a ventilator. This mother was married but her husband never came...

Premium Bachelor of Science in Nursing, Cystic fibrosis, Human 3510  Words | 10  Pages

Open Document

Pediatric Respiratory Disorders

to identify cystic fibrosis Sputum Culture -identifies pathogens -collect early in morning -use nasal or gastric washings for children too young to produce sputum Pulse Ox-measures O2 saturation of blood using infrared light Pediatric Respiratory Assessment: Exam PHYSICAL EXAM Chest diameter: anterior & posterior diameter should be = until 2 yrs. If = beyond 2yrs it could be a sign of CHRONIC OBSTRUCTIVE LUNG CONDITIONS known as the "barrel chest" seen in CYSTIC FIBROSIS & ASTHMA...

Premium Acute respiratory distress syndrome, Asthma, Cystic fibrosis 4669  Words | 13  Pages

Open Document

Clients with Disabilities

Cystic Fibrosis: Description, signs and symptoms: Cystic fibrosis is a genetic disorder, which is acquired at conception and therefore present at birth. The disorder is entirely caused by one pair of genes. People with cystic fibrosis produce abnormally thick, stick mucus in the linings of internal organs such as the lungs and intestines. The most common signs are persistent coughing, excessive sweating leading to salty skin, huge appetite but poor weight gain, and pale, oily, very smelly faeces...

Premium Allele, Cystic fibrosis 4973  Words | 16  Pages

Open Document

Gene Therapy Market - Global Industry Analysis, Size, Share, Growth, Trends And Forecast, 2013 – 2019

Gene therapy involves use of DNA as a pharmaceutical agent to treat diseases. It is one of the most important developments in the field of medicine that has potential to treat various lethal diseases such as HIV, cancer and cystic fibrosis. In the long run, biotechnology and clinical trial industries will benefit from developments in gene therapy and provide potential treatment solutions for various incurable diseases. Browse Full Report with TOC: http://www.transparencymarketresearch.com/gene-therapy-market...

Premium Clinical data acquisition, Clinical trial, Cystic fibrosis 394  Words | 2  Pages

Open Document

Endocrine System

guideline manages to pack in complications in combination with diabetes and the special circumstances that need to be accounted for. This includes special recommendations for End-of-life care, disorders of the pancreas, older persons with diabetes, cystic fibrosis, coeliac disease, pregnancy, antenatal care, post-natal care, HIV, eating disorders, and fasting. In conclusion, this article has given many different guidelines for care and prevention of diabetes. The article summarized some of the UK’s general...

Premium Cystic fibrosis, Diabetes mellitus, Diabetes mellitus type 1 475  Words | 2  Pages

Open Document

Booooooooo

calories and nutrients Older adults People who are taking medicines that decrease appetite or affect the digestion and absorption of nutrients People who abuse drugs or alcohol People with eating disorders People with certain diseases such as cystic fibrosis, celiac disease, liver disease, kidney disease and cancer People with a low income who have trouble buying the right kind of food Pregnant women (Healthtouch, 2007) References   Healthtouch. (2007). Malnutrition. Retrieved May 12...

Premium Appetite, Cancer, Cystic fibrosis 365  Words | 2  Pages

Open Document

Become a StudyMode Member

Sign Up - It's Free