Dr. Paul Quinton, who has CF himself, discovered that the basic defect in the CF sweat duct was due to anion impermeability and not defective anion exchange. His discovery is considered to be one of the major advances in understanding the basic CF defect.
Dorothy Hansine Andersen was the first person to identify the symptoms of CF.
well actually...... united stated and canatian research team found it found in the 1930's or around there
Lap-Chee Tsui and Dr. Francis Collins
1930s - 1940s
An excellent source of information on cystic fibrosis, the Cystic Fibrosis Foundation can be accessed in a number of ways. Information on a local chapter can be accessed via phone at 800-344-4823.
well go to webmd.com and find out
Unfortunately, cystic fibrosis cannot be cured. There is medication getting better all the time but now, the government in the UK have not funded in any cure. This means that in the UK, we may only find a cure if a devoted medical professional actually spent his own time to find the cure
Most people who have this disease die around 35 .
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.
You can find information about holistic medicine for acne and cystic fibrosis on the following website: http://www.holisticonline.com/remedies/acne.htm. They have a lot of useful info.
phenotypes are decided by the alleles for that particular characteristic, by a dominant or two recessive alleles. For example, cystic fibrosis has a recessive allele so the phenotype of cystic fibrosis would only appear if there were two of the recessive allele, one from each parent, were present. A heterozygous carrier of the cystic fibrosis allele would show the phenotype of not having cystic fibrosis. So to determine the phenotype simply find out which allele is dominant and find what alleles each parent has the the probability of each phenotype can be calculated
take a genetic test - a blood or tissue sample is analysed for specific mutations
There will be a cure when there are more people with it and there is alot more funding for research. As for now, people are busy trying to find cures for cancer. The numbers of patients with cancer out weigh those with Cystic Fibrosis, therefore Cystic Fibrosis research is given less financial aid. It has to do with numbers. Also waiting on improved technology as always.
Analysis of the cells from the chorionic villus enables the detection of over 200 diseases and disorders such as Down Syndrome, Tay-Sachs disease, and cystic fibrosis
Analysis of the cells from the chorionic villus enables the detection of over 200 diseases and disorders such as Down Syndrome, Tay-Sachs disease, and cystic fibrosis
You can register with the Cystic Fibrosis Foundation and they will send you free address labels within 4 to 6 weeks. You will have your choice of the Roses or America design.