DISEASE
        Cystic fibrosis is an autosomal recessive trait on chromosome 7. This dis locate ventures chloride transport resulting in abnormal mucus production. This lifelong indisposition usually gets more severe with age and can affect two males and females. Symptoms and severity differ from person to person. Cystic fibrosis is the most common fatal inherited disease among whites and the major fetch of chronic lung disease in children. 50% of people atomic number 18 expected to live to be 30, but a mass die before age thirteen. 1:2000 whites eat up cystic fibrosis, 1:17000 blacks, 1:6000 live births, 1:2500 Americans, and 1:20 is a carrier.
        The constituents are inherited in pairs, with one divisor coming from each(prenominal) parent to make the pair. Cystic fibrosis occurs when both genes flip mutations. A person with cystic fibrosis receives one cystic fibrosis gene from each parent. The parents of a child, with cystic fibrosis, each defy one nonworking replica of the gene and one working copy of the gene. The parents are called cystic fibrosis carriers, and because they have one working gene they have no symptoms.
Carrier parents have 1:4 come about to have a child who is a noncarrier of cystic fibrosis, a 1:2 chance to have a child who carries the gene, and a 1:4 chance with each pregnancy to have an affected child. If you have a son or daughter with cystic fibrosis, then you have a 1:1 chance of cosmos a carrier. If you have a brother or sister with CF, you have a 2:3 chance of being a carrier. If you have a niece or nephew with CF, you have a 1:2 chance of being a carrier. If you have an aunt or uncle with CF, you have a 1:3 chance of being a carrier and a 1:4 chance if you have a...
If you want to get a full essay, wisit our page: write my paper
No comments:
Post a Comment