the gene that codes for an important cell membrane protein called cystic fibrosis transmembrane conductance regulator CFTR which acts as a chloride channel to transport chloride ions in and out of the epithelial cells in GIT and respiratory tract and also cells of sweat glands .
Cystic fibrosis (CF) is an inherited disease that causes the body to produce mucus that's extremely thick and sticky. The mucus is thicker than normal because CF affects cells in the epithelium(pronounced: eh-puh-THEE-lee-um), the layer of cells that lines the passages in the body's organs.
Both parents had at least one allele for cystic fibrosis.
The lungs (pulmonary surfactant is missing or diminished).
Yes. A person can have a baby with cystic fibrosis at any age.
Cystic Fibrosis is a cronic illness meaning that if you look at a person you cant tell the diff between a cf person
Let's call the gene "C." Capital C means no cystic fibrosis; lower c means cystic fibrosis, since it is a recessive gene. CC is a person who does not have cystic fibrosis and also is not a carrier. Cc indicated a carrier. cc shows a person with cystic fibrosis. In order for a child to have cystic fibrosis, its parents must be: 1. cc and cc (both have cystic fibrosis, so every child will as well.) 2. Cc and Cc (both carriers; 25% chance of having a child with cystic fibrosis) 3. Cc and cc (one parent is a carrier and one has cystic fibrosis; there is a 50% chance that the children will have cystic fibrosis.)
phenylalanine
Cystic fibrosis is a inherited disease where ususally by the time of 30-35 the person who has it does die.
What is cystic fibrosis? Cystic fibrosis is a life threatening disease.
Cystic fibrosis has no cure. However, treatments have greatly improved in recent years. Early treatment for cystic fibrosis can improve both quality of life and lifespan.
The genotype of a person with CF is cc. The genotype of a carrier of a CF mutation is Cc.
cystic fibrosis (:cystic fibrosis :)cystic fibrosis ^-^
The Same Way Any other person would get CF (Cystic Fibrosis), although it's Very Rare For African Americans to get it. Cystic Fibrosis is most common among Caucasians.