There are no symptoms or anything in a carrier of cystic fibrosis. The only way to find out is to get tested, or if you have a child with cystic fibrosis, you must be a carrier, as well as your partner.
yes although if someone in your family has cf you can go to the doctors and get tested. aparently some carrriers have cf symptoms too
You can and you can't die from Cystic Fibrosis........ like if your a healthy case of cystic fibrosis you can't really die but you still can ....and if you asking well how you know......I know because I have cystic fibrosis
Most people who have this disease die around 35 .
sorry lave i dont know !
Good Question. The answer is cystic fibrosis is not contagious, however, people with cystic fibrosis tend to carry bacterial infections that can cause serious issues to other people with CF, so infection control procedures should be used when two or more cystics are around each other. General population folks need not fear of getting cystic fibrosis from others - it's a hereditary disease.
I dont know someone help?
More than 1,000 different mutations in the CFTR gene have been identified in cystic fibrosis patients. The most common mutation (observed in 70% of cystic fibrosis patients) is a three-base deletion in the DNA sequence, causing an absence of a single amino acid in the protein product. About 2,500 babies are born with cystic fibrosis in the U.S. each year. More than 10 million Americans carry the cystic fibrosis gene but don't know it.
i dont know eat a potato OH, and how did you remember how to spell that
Cystic Fibrosis cannot be prevented. It is an inherited disease, so there is no possible way to prevent something inherited. One parent will be a carrier and so will the other parent, therefore resulting in the child having CF.
The prevalence of CF carriers (meaning they carry one mutation) is 1 in 25 in the Caucasian population. Most people don't even know that they are carriers until they have a child with CF. That means that the CF allele can unknowingly be passed down through generations. Carriers are typically asymptomatic and there is evidence to support that the CF mutation protected our ancestors from fatal diseases. So natural selection actually played a role in the proliferation of CF carriers.
you take creon its a capsule filled with tiny tan beads you open up the pill and swallow the beads on the inside the beads are real tiny so its easy and they have no taste so u dont hafe to worry i know cause i have cystic fibrosis
i want to know too
Cystic fibrosis can be detected days after birth in several ways: Babies can present with symptoms particular to CF or they can be screened for CF as part of a state/provincial health policy. The 'sweat' test is often used as a determinant of CF.