Cystic Fibrosis
About 1 out of 201 Caucasian people carries at least one of the fatal defective genes that cause cystic fibrosis, CF, or mucoviscidosis (in Europe) although carriers don't show any signs of the disease. Therefore, 10 million2 people carry the defective gene and aren't aware of it. Consequently, it makes it one of the most common genetic defect in the United States. CF is a autosomal recessive gene. That means that it may, but doesn't always skip generations. In order to get this disease, both parents must be carriers. If one parent has CF and the other one is not a carrier than there is a 100% chance that their child will be a carrier. If one parent has CF and the other is a carrier than the child has a 50% chance of having CF and a 50% chance of just being a carrier. If both parents are carriers than their child will have a 25% of having CF, a 50% chance of being a carrier and a 25% chance of not being affected. CF is common in both males and females, there is not a specific sex that it is more common in. How does a person know if they have CF? There are many symptoms to this deadly disease including: salty tasting skin, constant coughing, large amounts of mucus, trouble gaining weight, frequent greasy, foul sme
Doctors have many "delivery vans" that deliver the good genes. Doctors transport vigorous process and puts the mother's health at risk. It may also be hard for a women to get pregnant though because the mucus blocks the sperm from entering the uterus the to the fallopian tubes. About 98% of men with CF are infertile8. Even though sperm are produced, they can't get to the semen because the vas definers is blocked. In some new research, it has been thought that men who are sterile have a different form of CF that oesn't involve the digestive system and the lungs. need to have all the symptoms in order to have cystic fibrosis, but they usually show most of them. Another way are different genetic testing. Doctors can now do genetic testing for CF, but about 10 years ago they couldn't. In 1989, the location where the of the defective gene on chromosome number 7 is was discovered by Francis S. Collins from University of Michigan. Tests can now be taken to see if an unborn child is infected with CF such tests are amniocentesis, chronic villus biopsy3 and a removal of cells from the embryo during invitro. Now there are many tests that can be done to find put if a person has CF. Also CF affects the digestive tract. The overproduction of mucus causes the Furthermore CF causes the sweat glands to release about 5 times6 as much salt as normal. In a normal person, mucus in the lungs helps get rid of germs and bacteria in
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Approximate Word count = 2306
Approximate Pages = 9 (250 words per page double spaced)
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