

1.) Cystic Fibrosis is a disease that causes mucus to build up in the lungs, airways, and digestive system.
2.) Officially, Cystic Fibrosis was not discovered until the 1930's when the earliest paper on the disease was written by Dr.Fanconi, a Swiss pediatrician. However, there has been suspicion of it sense the early 1700's including an old German saying, "A child whose forehead tastes like salt when kissed will soon die."
3.) Symptoms include delayed growth, salty tasting skin, cubed fingers, no bowel movements in the first 24-48 hours of life, failure to gain weight during childhood, belly pain, fatigue, coughing, and shortness of breath.
4.) It is caused by a defective gene and id recessive.
5.) There are tests to detect the cf gene including a blood test and a test that measures salt levels in sweat.
6.) There are many treatment options depending on the severity of the case. Inhaled medicines, antibiotics, and in severe cases, lung transplants are options.
7.) Cystic Fibrosis cannot be prevented.
8.)Currently the Scripps Research Institute is leading research on Cystic Fibrosis.
Cystic Fibrosis Foundation
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