Cystic Fibrosis
A detailed Summary of Cystic Fibrosis
About 1 out of 201 Caucasian people carry 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 million people carry the defective gene and don't know it. Consequently, it is one of the most common genetic defect in the United States.
Cystic fibrosis is a autosomal recessive gene. That means that it may, but doesn't always have to skip generations. In order to have this disease, both parents must be carriers. If one parent has Cystic fibrosis 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 Cystic fibrosis 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 bein

One way which CF can be detected is to observe the symptoms. A person doesn't 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.
There are now many drugs that are in the market and many more that are in development. Treatments mainly depends on what organs are effected. The first new drug therapy in 30 years was approved by the Food and Drug Administration in December of 93'. It's a mucus-thinning drug called Pulmozymec. Pulmozymec has reduced the number of respi
Some common words found in the essay are:
Pulmozymec Pulmozymec, United Cystic, Cystic Fibrosis, Michigan Tests, CF CF, cystic fibrosis, Administration December, 50% chance, cf 50% chance, cystic fibrosis carrier, parent cystic fibrosis, chance carrier, 50% chance carrier, cf 50%, parents carriers, people carry, genetic testing, defective gene, fibrosis carrier, parent cystic,
Approximate Word count = 650
Approximate Pages = 3 (250 words per page double spaced)
Category: Science
Saved Paper
Newest Essays
- My Personal Value System
- Iraq and High Energy...
- The Development of English...
- Critique of a Research...
- Visiting the Elderly in...
- Ad Critique: Peters, Jeremy...
- Catell's Structure-Based...
- Current Diabetes Epidemic:...
- Job Search: Push Pull...
- Proposal: Social...
Testimonials
-
"Thank You So Much!!! You have saved me once again!!!"
Jack M. -
"With so many papers to chose from, I was able to get ideas to help me with all of my classes. Thank You!"
Brian P. -
"I've used this site for the last 3 years to help me come up with ideas for my papers."
Sara J. -
"I use this site every week to help me write my own papers!"
Rachel W. -
"I love this site!!!"
Marie N.
