No cystic fibrosis is caused by a mutated CFTR gene.
Assuming that each parent is a carrier for cystic fibrosis (has the genotype Ff), the probability that their second child will develop cystic fibrosis is one fourth. The probability doesn't change with the number of children they have. For each pregnancy, the chance that the child will have cystic fibrosis (have the genotype ff) is exactly the same.
The sequence of amino acids in cystic fibrosis is caused by a mutation in the CFTR gene, which leads to the production of a faulty cystic fibrosis transmembrane conductance regulator protein. This mutated protein results in abnormal function, leading to the characteristic symptoms of cystic fibrosis such as thick mucus production.
Two genetic disorders are Turner's syndrome and cystic fibrosis.
Karyotyping looks at the complete set of chromosomes. It can detect large-scale abnormalities, such as missing/extra chromosomes or whether large pieces of chromosomes have been rearranged. It cannot detect any of the many, many genetic disorders which are caused by a single gene, several genes or gene interactions. Examples of these would be cystic fibrosis, sickle-cell disease and dwarfism.
i copied the following answer from health.howstuffworks.com Unlike some other genetic conditions, cystic fibrosisoccurs equally as often in men and women. The genetic mutation for cystic fibrosis occurs on chromosome 7 and is not impacted by gender. The severity of symptoms related to cystic fibrosis, however, does vary in men and women. In particular, girls with cystic fibrosis have more difficulty with meeting growth milestones and experience more lung-related problems compared to boys. Due to these more severe symptoms, women with cystic fibrosis have shorter life expectancies than men. It is estimated that men with cystic fibrosis live four to five years longer than women with cystic fibrosis, Moreover, under the age of 20, girls have a 60 percent greater chance of dying due to cystic fibrosis complications compared to males [source: Cystic Fibrosis Worldwide]. As a result, the prevalence of male adults with cystic fibrosis is greater than the prevalence of female adults with cystic fibrosis, suggesting a male advantage with the disorder. Cystic fibrosis researchers argue that this gender difference is the result of early-onset lung infections in girls. Girls appear to develop these infections earlier in life than boys, leading to more severe cystic fibrosis complications, and even death. Girls also appear to have greater difficulty maintaining a healthy body weight after puberty compared to males, which places girls at greater risk for cystic fibrosis complications. It appears that this gender gap can narrow if girls are provided with more intensive medical care. In fact, girls and women who receive regular intravenous antibiotics, regardless of their condition, have improved survival rates [source: Cystic Fibrosis Worldwide]. As a result, countries with excellent health care, such as Scandinavian countries, do not have a difference in the survival rate of men and women with cystic fibrosis. i hope it helps:)
Neither. Cystic fibrosis is caused by genetic mutations on chromosome 7.
What is cystic fibrosis? Cystic fibrosis is a life threatening disease.
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Is a carrier of cystic fibrosis
Yes, girls can get cystic fibrosis.
To found Cystic Fibrosis, watch Princess and I!!!
No, there is currently no cure for cystic fibrosis.
No. Cystic fibrosis is a genetic disease.
cystic fibrosis foundation
No. Cystic fibrosis is a genetic disease.
The term that best describes the inheritance of cystic fibrosis is that it is genetic. Cystic fibrosis is caused by recessive alleles. Cystic fibrosis is an autosomal recessive genetic disease.
Cystic Fibrosis is a genetic disorder, 2 parents have a CF gene, if their offspring inherits that trait they will have Cystic Fibrosis.