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Cystic Fibrosis: usually from both parents,  usually affect both,  signs and symptoms- Very salty-tasting skin.

Persistent coughing, at times with phlegm.

Frequent lung infections including pneumonia or bronchitis.

Wheezing or shortness of breath.

Poor growth or weight gain in spite of a good appetite.

Frequent greasy, bulky stools or difficulty with bowel movements.

Male infertility.  frequency- Frequency. Cystic fibrosis is a common genetic disease within the white population in the United States. The disease occurs in 1 in 2,500 to 3,500 white newborns. Cystic fibrosis is less common in other ethnic groups, affecting about 1 in 17,000 African Americans and 1 in 31,000 Asian Americans. treated- antibiotics to prevent and treat chest infections. medicines to make the mucus in the lungs thinner and easier to cough up. medicines to widen the airways and reduce inflammation. special techniques and devices to help clear mucus from the lungs. Average life- Today, the average life span for people with CF who live to adulthood is about 44 years. Death is most often caused by lung complications. birth- Prenatal diagnostic tests to detect CF and other disorders include amniocentesis and chorionic villus sampling (CVS). Amniocentesis usually is done between 15 and 20 weeks of pregnancy, but it also can be done up until you give birth.  Your doctor may perform a prenatal screening to test for CF if both parents know they carry the gene. This is performed while you are pregnant. It checks for any health problems with your baby before he or she is born. The screening also can detect other genetic disorders

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