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What else can I help you with?
How many center in Pakistan on cystic fibrosis?
There is no cystic fibrosis centre in pakistan But Agha khan hospital karachi is best to diagnoseand treat cystic fibrosis patients .Almost all the medications of cystic fibrosis are available in Pakistan.
How long does cystic fibrosis last?
The person who has Cystic Fibrosis has it for life.
What disease is called by a genetic mutation?
cystic fibrosis
is cystic fibrosis affect the human body?
Cystic fibrosis is widely recognized as a lung disease, but it is actually a disease that affects many parts of the body. So yes. it can:) hope this is helpful
Does religion have an impact on cystic fibrosis?
Unfortunately, cystic fibrosis cannot be cured by prayer. If it could be cured by prayer, the disease would have disappeared a long time ago, because there are a great many people praying all the time. We have a great abundance of prayer, in this world. But we still have cystic fibrosis.
How many people have cystic fibrosis in Europe in the year 1985?
1 in every 8000
How many people die of cystic fibrosis a year?
go to www.cdc/gov.com :D hope i helped
How many people in Mississippi have cystic fibrosis?
Cystic fibrosis (CF) is a rare genetic disorder, and its prevalence can vary by region. In Mississippi, it is estimated that there are approximately 100 to 200 individuals living with cystic fibrosis. The exact number can fluctuate due to factors such as population size and the availability of medical resources. For the most accurate and up-to-date information, it is advisable to consult local health departments or CF registries.
How many exons are in CFTR?
The CFTR (cystic fibrosis transmembrane conductance regulator) gene contains 27 exons. These exons encode the protein responsible for regulating chloride ions across epithelial cell membranes, and mutations in this gene are associated with cystic fibrosis.
How many copies of cystic fibrosis do you need to suffer from?
Cystic fibrosis (CF) is an autosomal recessive genetic disorder, meaning that a person must inherit two defective copies of the CFTR gene—one from each parent—to develop the disease. If an individual has only one copy of the mutated gene, they are considered a carrier but will not show symptoms of the disease. Therefore, you need two copies of the mutated gene to suffer from cystic fibrosis.
How many people died from cystic fibrosis in each year?
Deaths from Cystic Fibrosis: 485 deaths (NHLBI 1999)Death rate extrapolations for USA for Cystic Fibrosis: 484 per year, 40 per month, 9 per week, 1 per day, 0 per hour, 0 per minute, 0 per second. Note: this extrapolation calculation uses the deaths statistic: 485 deaths (NHLBI 1999)45 people died from cystic fibrosis in Australia 2000 (Australia's Health 2004, AIHW)Source(s):RRT
What is the risk in each pregnancy of having a child with cystic fibrosis?
By "another pregnancy", I assume that the parents have had one child with cystic fibrosis. As cystic fibrosis is recessive and neither parent suffers from it, they must both be carriers. That means the chances of the next baby having CF is 25%, or a one in four chance. Assuming both parents have one CF and one non-CF gene, the combinations work out: non-CF x non-CF (normal) non-CF x CF (carrier) CF x non-CF (carrier) CF x CF (cystic fibrosis sufferer) Therefore their chances of having a: normal child = 25% child who is a CF carrier = 50% child who suffers from CF = 25%
