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.
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.
The person who has Cystic Fibrosis has it for life.
cystic fibrosis
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
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.
Both cystic fibrosis and sickle cell anemia are single mutation diseases - one mutation in a single gene is enough to cause the disease. However, for cystic fibrosis both alleles of the gene must be mutated for the disease to develop. For sickle cell anemia, only one allele can carry the mutation and some signs of the disorder will be present. Having two alleles with the mutation causes much more significant disease.
1 in every 8000
go to www.cdc/gov.com :D hope i helped
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.
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.
There are no 'Side Effects', just things that 'come with the package'. You can suffer breathlessness, bowel problems and probalmes with liver and kidneys. There are other things too, but at age 13, that's all I've really had so far.
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