What is a cystic fibrosis carrier?

Cystic fibrosis of the carrier is a person who has a mutation that causes cystic fibrosis in its genes, but has no disease. Each person has two genes of transmembrane controller of cystic fibrosis. If there is one normal gene of the transmembrane regulator of cystic fibrosis and the other is mutated, the person is a carrier. A person whose genes of cystic fibrosis of transmembrane regulator are mutated will have cystic fibrosis.

In order for a child to be born with cystic fibrosis, the child must inherit the mutated gene from each parent. This means that the child cannot be born with cystic fibrosis if both parents are not carriers. If the child only inherits the mutated gene of the transmembrane regulator of cystic fibrosis from the mother or father, the child will be a carrier of cystic fibrosis. Although both parents are carriers, the child does not necessarily have cystic fibrosis or even be a cystic fibrosis, because the child could inherit one normal gen.m both parents.

There are no health risks associated with a cystic fibrosis carrier. Many people walk their entire lives without knowing they are carriers. Couples trying to conceive or have recently become pregnant can undergo genetic testing through saliva or blood to determine whether any of them is a carrier. Because there are many different types of mutations, a few rare can be not detected by testing the carrier. If both parents are carriers, the fetus can be tested for this disease while in the womb, if parents want it.

anyone can be a carrier of cystic fibrosis, but it is more common that the Caucasians have a mutated gene. People of Asian origin are least likely to carry this property. Different carriers have different mutations, which can lead to different symptoms and level of severity of cystic fibrosis for a child born with disease.

babies born with cystic fibrosis require special medical care, which is one of the reasons why many parents decide to seeStit whether they are cystic fibrosis carriers before birth. If both parents are carriers and a child has a cystic fibrosis, parents can prepare consulting with doctors and specialists to prepare for treatment that the child will require. Although there is no cure for cystic fibrosis, many people with this disease live up to their 40 or 50 years with proper care and medicines.