What is cystic fibrosis?
Cystic Fibrosis Foundation - Frequently Asked QuestionsCystic fibrosis is a life-threatening disease that causes mucus to build up and clog some of the organs in the body, particularly in the lungs and pancreas. When mucus clogs the lungs, it can make breathing very difficult. The thick mucus also causes bacteria (or germs) to get stuck in the airways, which causes inflammation (or swelling) and infections that leads to lung damage. Mucus also can block the digestive tract and pancreas.
Related QuestionsHow do people get cystic fibrosis?
Cystic Fibrosis Foundation - Frequently Asked QuestionsCystic fibrosis is a genetic disease. That means people inherit it from their parents through genes (or DNA), which also determine a lot of other characteristics including height, hair color and eye color. Genes, found in the nucleus of all the body's cells, control cell function by serving as the blueprint for the production of proteins. The defective gene that is responsible for causing cystic fibrosis is on chromosome 7.
Related QuestionsWho gets cystic fibrosis?
Cystic Fibrosis Foundation - Frequently Asked QuestionsApproximately 30,000 people in the United States have cystic fibrosis. An additional ten million more—or about one in every 31 Americans—are carriers of the defective CF gene, but do not have the disease. The disease is most common in Caucasians, but it can affect all races. The severity of cystic fibrosis symptoms is different from person to person.
Related QuestionsIs cystic fibrosis fatal?
Cystic Fibrosis Foundation - Frequently Asked QuestionsCurrently, there is no cure for cystic fibrosis. However, specialized medical care, aggressive drug treatments, and therapies, along with proper CF nutrition, can lengthen and improve the quality of life for those with CF. The best way for people with cystic fibrosis to fight their disease is to work with their medical caregivers at a CF Foundation-accredited care center. The care center partners with people who have CF to help keep them in the best health possible.
Related QuestionsWHAT IS CYSTIC FIBROSIS? WHO SHOULD BE TESTED?
Medical On-line Reference GuideDental X-rays- Dental caries- Dental injuries -Dental plaque identification procedure and removal Denture problems American Diabetes Assoc. - self assessment test that will help determine whether yu are at high risk, how to reduce your risk through exercise and diet.
Related QuestionsMySpace.com Blogs - Lissa MySpace BlogCystic fibrosis (CF) is a life-threatening disease that causes mucus to build up and clog some of the organs in the body, particularly in the lungs and pancreas. When mucus clogs the lungs, it can make breathing very difficult. The thick mucus also causes bacteria (or germs) to get stuck in the airways, which causes inflammation (or swelling) and infections that leads to lung damage. Mucus also can block the digestive tract and pancreas.Related Questions
Cystic Fibrosis - Questions & AnswersCystic Fibrosis (CF) is an inherited disease that causes the glands that make mucous, saliva and sweat to not work properly. The mucous is sticky instead of thin and slippery and chokes the lungs and can block openings in other major organs, which makes it difficult to break down and absorb food. CF can cause permanent liver damage.Related Questions
Quality Health | Cystic FibrosisCystic fibrosis is a disease that causes mucus in the body to become thick, dry, and sticky. This glue-like mucus builds up and causes problems in many of the body's organs, especially the lungs and the pancreas . People who have cystic fibrosis can have serious breathing problems and lung disease. They can also have problems with nutrition, digestion, growth, and development. There is no cure for cystic fibrosis and the disease generally gets worse over time.Related Questions
What is Cystic Fibrosis and Male Infertility?
Untitled DocumentMen who have cystic fibrosis often have a congenital anomaly in the male genital tract. The vas deferens, the tube connecting the testicle and epididymis to the ejaculatory duct, is congenitally absent. This makes it impossible for the sperms to pass through the penis. Using testicular sperm aspiration, the urologist can obtain sufficient sperm to allow excellent success with IVF and ICSI (intracytoplasmic sperm injection).
Related QuestionsWhy not add screening for cystic fibrosis?
Texas Department of State Health Services - FAQs about Newbo...The 79th Texas Legislature in 2005 mandated that DSHS expand to the ACMG-recommended panel of disorders as funding allowed and appropriated $3.1 million. The startup funding allows 20 additional disorders to be added to the screening panel. Cystic fibrosis startup would require an additional $2 million to $3 million.
Related QuestionsHow Common is Cystic Fibrosis?
Cystic Fibrosis - Questions & AnswersCF is one of the most common inherited diseases of Caucasians (whites). CF occurs in one of every 3,200 live Caucasian births. It occurs in one in every 15,000 live African-American births. CF is uncommon in Asians and most Native American tribes. It is being seen more often in Hispanics. CF affects almost every race. About 1,000 new cases of CF are diagnosed each year.
Related QuestionsCan I "Catch" Cystic Fibrosis?
Cystic Fibrosis - Questions & AnswersNo. CF is a disease that a person is born with. It comes from a defective gene from each parent. Genes are the main unit of heredity. Not all people carry the defective gene that causes CF, so if one parent has the gene and the other does not, the child will not have CF. You cannot control which genes get passed to your child.
Related QuestionsWhat Are the Symptoms of Cystic Fibrosis?
Cystic Fibrosis - Questions & AnswersPeople with CF can have several symptoms including very salty-tasting skin; steady coughing at times with phlegm; wheezing or shortness of breath; a huge appetite but remains thin; and large, greasy stools. These symptoms are different from person to person.
Related QuestionsHow Is Cystic Fibrosis Diagnosed?
Cystic Fibrosis - Questions & AnswersThe main test for CF is called the sweat test and it measures the amount of salt in sweat. Starting in 2002, all babies born in New York State are tested at birth as part of a series of tests on newborn babies. If there is reason to think a child has CF, the test should be done in an accredited CF Care Center.
Related QuestionsHow Is Cystic Fibrosis Treated?
Cystic Fibrosis - Questions & AnswersThere are many treatments for the symptoms and CF related problems. Treatment is aimed at preventing lung infections, reducing the amount and thickness of mucous in the lungs, improving airflow and maintaining nutrition.
Related QuestionsIs There a Cure For Cystic Fibrosis?
Cystic Fibrosis - Questions & AnswersThere is no cure for CF at this time, but ongoing research has led to advances in treatment, which have significantly improved the lives of many CF patients. New discoveries in the treatment of CF have helped people with the disease live longer. Twenty years ago, only half the people with CF lived beyond age 21, but today half the people with CF live past 35 years of age.
Related QuestionsHow Do We Inherit Cystic Fibrosis?
Open Directory - Science: Biology: Genetics: Eukaryotic: Animal: Mammal: Human: Testing and Counseling EBI, the European Bioinformatics Institute (EMBL Outstation, Hinxton, UK) serving the bioinformatics community
Related QuestionsAre any results of the cystic fibrosis Phase 2a trials available?
PTC TherapeuticsIn November 2006, we presented data from the PTC124 cystic fibrosis clinical trials in Israel and the U.S. Cystic fibrosis is caused by a lack of the cystic fibrosis transmembrane conductance regulator (CFTR) protein. To determine whether PTC124 was inducing production of active CFTR protein in patients, we measured nasal transepithelial potential difference (TEPD).
Related QuestionsWhere can I find more information about Cystic Fibrosis and its causes?
Pseudomonas Genome Database - Frequently Asked QuestionsVisit the Cystic Fibrosis Foundation website for information and links to further resources on this disease. For more detailed information, including discoverer Riordan et al., please read the following articles at NCBI. PathoGenesis Corporation, who played a major role in sequencing the first P. aeruginosa genome, is now a part of Chiron and continues its interest in the development of new anti-Pseudomonad drugs.
Related QuestionsWhat causes cystic fibrosis?
Quality Health | Cystic FibrosisCystic fibrosis is a genetic disorder. A child must inherit a specific gene from both parents to get cystic fibrosis.
Related QuestionsWhen will all babies be screened for cystic fibrosis?
UK Newborn Screening Programme Centre: FAQsScreening for cystic fibrosis is being phased in gradually throughout the UK. All newborn babies should be routinely screened for cystic fibrosis by April 2007.
Related QuestionsDo you serve children with Cystic Fibrosis (CF)?
Victory JunctionWe are able to serve children with CF on a limited basis. Our Medical Advisory Board and Medical Team have determined that we can accept one child (or siblings) with CF for each of our Summer Sessions. The application process is the same and our medical team will review each application as it is received.
Related QuestionsWhat precautions should be taken in patients with cystic fibrosis?
Learning Through Questions With Assista at Conceptualist.com...How does Assista compare to Yahoo Answers? First, these are totally different systems. “Yahoo Answers” is more of a Q&A type site where they only list questions from their own database while Assista aggregates content (questions) from every web page on the internet, including all of “Yahoo Answers” questions.
Related Questions