The History of Cystic Fibrosis

The History of cystic Fibrosis
What is cystic fibrosis? Cystic fibrosis is ca usaged by a mutated constituent. A person diagnosed with cystic fibrosis inherits two mutated cf genes, sensation from each p atomic number 18nt. Everyone who has cystic fibrosis was born with it. After birth cystic fibrosis cannot be developed nor can it be contagious.
People with cystic fibrosis have a variety of symptoms. Some cases be severe, small-arm others are mild. It is not curable, besides it is treatable. Scientist and doctors believe that there are more than one thousand ways the cf gene can mutate and the various mutations could cause the different symptoms. The cf gene that has the scientific name ABCC7 makes a protein called CFTR (cystic fibrosis transmembrane conductance regulator). The CFTR protein is found in cells called epithelial cells which form a lining inside umteen organs.
Sometimes cystic fibrosis is diagnosed before a baby is born, but many infants are diagnosed shortly after birth. Most infants with cystic fibrosis are born with Meconium Ileus. Most infants without this condition are diagnosed tetrad to six weeks later when parents and doctors notice that the infant coughs frequently, and has not gained weight, eve though it is eating enough. To test for cystic fibrosis, doctors often use a basic test called a sweat test.




Cystic fibrosis has been affecting humans since the middle ages. Cystic fibrosis was unstudied until the early on 1900s.
Without testing every person before they become a parent there is no way to prevent cystic fibrosis, unlike other diseases. Most genetic test are not accurate.
Cf has many symptoms that call for many intercessions. to each one person with cf has different needs, and anyone with cf should become the treatment very seriously.
Chest physical therapy (PT) is one of the most burning(prenominal) treatments for CF. It helps get rid of it before germs can take hold and cause infections, and shakes loose the thick mucus in the lungs.
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