Role Genetics play in Disease

Cystic fibrosis is an autosomal recessive exocrine gland disease that affects various organ systems, notably the gastrointestinal and respiratory systems (McCane & Huether, 2019). Cystic fibrosis is an autosomal recessive condition, which implies that a person must be homozygous for the recessive gene to develop the disease. In another way, each individual has two genes that express qualities. If both parents have one gene that causes Cystic Fibrosis, they are both carriers. When they have a child, each of them passes on the gene that causes Cystic Fibrosis to their kid, and the child ends up with two genes that cause CF. When two people who are heterozygous carriers of CF have a child, there is a 25% risk that the kid will have CF. Furthermore, if two individuals with CF have a kid, all of their offspring will inherit the CF gene.

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Role Genetics play in Disease
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