Yes but depending on your age and the risk you are willin to take
Men and women are equally likely to inherit this.
Cystic Fibrosis is more prevalent among people with European and Caucasian decent. 70,000 people worldwide suffer from the condition, and an estimated 2,500 Caucasians inherit the disorder.
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
Yes, since the disease is a recessive inherted trait BOTH parents must carry the gene but will not have the disease itself. Approximately 30,000 people in the United States have cystic fibrosis. An additional ten million more-or about one in every 31 Americans-are carriers of the defective CF gene, but do not have the disease. The disease is most common in Caucasians, but it can affect all races.
For a baby to be born with Cystic Fibrosis, both parents must be carriers of the faulty CF gene. Where both parents carry the faulty gene, each child has a one in four chance of having CF, a two in four chance of being a carrier and a one in four chance of not having any CF genes.
The general qualifications for donating eggs are quite strict. As well as being within normal weight, height, and IQ, they often will ask for a family history of any diseases, including cystic fibrosis. They would most likely refuse an egg donation from anyone with any diseases than could be passed on to a child.
Cystic Fibrosis can but not always lead to fertility problems. In most men with CF, the tubes that carry sperm are blocked, which causes infertility (approx 95%). Because underweight women are more likely to have irregular menstrual cycles, the nutritional problems associated with CF may affect fertility. hope this helps
fibrosis
Cystic fibrosis affects primarily lungs and pancreas, not immune system. But a patient affected is debilitated and it would decrease the fuction of various systems, like the immune A CF patient that has had a lung transplant would have an impaired immune system because of the medication given for rejection. The medication would suppress the immune system so that the patients' body would be more likely to accept the new organ(s), but also making the patient more susceptible to other illnesses.
DefinitionNeonatal cystic fibrosis screening is a blood test that looks for increased levels of immunoreactive trypsinogen (IRT), an enzyme produced by the pancreas. The test is performed on newborns to screen for cystic fibrosis (CF).Alternative NamesCystic fibrosis screening - neonatal; Immunoreactive trypsinogen; IRT testHow the test is performedA sample of blood is either taken from the bottom of the baby's foot of a vein in the arm. A tiny drop of blood is collected onto a piece of filter paper and allowed to dry. The dried blood sample is sent to a lab for analysis.How to prepare for the testThere is no special preparation needed.Some states include this test in the routine newborn screening tests that are done before the baby leaves the hospital.If you live in a state that does not perform routine CF screening, your health care provider will explain whether testing is needed.How the test will feelThe brief feeling of discomfort will probably cause your baby to cry.Why the test is performedChildren with CF who are diagnosed early in life and start treatment at a young age may have better nutrition, growth, and lung function. Newborn screening tests allow doctors to identify children with CF before they have symptoms.Normal ValuesNormal values vary from lab to lab. Ask your doctor or testing center for details.What abnormal results meanIt is important to remember that a positive screening test for cystic fibrosis does not diagnose cystic fibrosis. If your child's test is positive, further tests will be done to confirm the possibility of CF. Not all children with a positive screening IRT test have CF.What the risks areRisks associated with the test include:Infection (a slight risk any time the skin is broken)Anxiety over false positive testsFalse reassurance over false negative testsSpecial considerationsThe IRT level does not indicate the severity of the CF. False-positives may occur.ReferencesFarrell PM, Rosenstein BJ, White TB, et al. Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic fibrosis consensus report. Journal of Pediatrics. Aug 2008;153(2).
I am, so I guess yea...an adult with CF can be overweight. That doesn't mean our bodies are getting what we need out of what we eat or take...it just means that the fat is certainly getting absorbed, along with what is most likely a stock pile of sodium related water weight.
Inbreeding has the effect of maintaining genetic defects in the bloodline. For example some human populations are descended from a limited genetic stock and have a high incidence of particular types of cancer and other diseases carried by defective genes, such as hemophilia, sickle-cell anemia and cystic fibrosis.