CF is caused by a defective chloride ion channel. There's a mutation in gene that codes for the protein which forms the channel. Chloride ions pass through it.
The gene on chromosome 7 produces a protein called cystic fibrosis trans-membrane regulator. Mutation in the DNA level of chromosome 7 leads to the absence of this protein which leads to cystic fibrosis. Cystic fibrosis is a recessive disease.
the symptoms of cystic fibrosis are has chesty coughs and feeling very flemmy. struggling to breath can also be a sign and mucus will fill the lungs and cover the throat.
The most common symptoms of Cystic Fibrosis are:Very salty-tasting skinPersistent coughing, wheezing or shortness of breathExcessive appetite but poor weight gainGreasy, bulky stools
The sequence of amino acids in cystic fibrosis is caused by a mutation in the CFTR gene, which leads to the production of a faulty cystic fibrosis transmembrane conductance regulator protein. This mutated protein results in abnormal function, leading to the characteristic symptoms of cystic fibrosis such as thick mucus production.
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.
What is cystic fibrosis? Cystic fibrosis is a life threatening disease.
cystic fibrosis (:cystic fibrosis :)cystic fibrosis ^-^
Cystic fibrosis
Yes, girls can get cystic fibrosis.
Is a carrier of cystic fibrosis
Cystic fibrosis currently does not have any sort of cure. Treatment is mainly done to reduce symptoms and complications. Treatment options include antibiotics, mucus-thinning drugs, and oral pancreas enzymes.
Cystic fibrosis is the genetic disorder that occurs when the body produces abnormally thick mucus. This condition affects the lungs, digestive system, and other organs, leading to recurrent infections and difficulty in breathing and digesting food.