Cystic fibrosis is an autosomal recessive disorder caused by mutations in the CFTR (cystic fibrosis transmembrane conductance regulator) gene. Heterozygous carriers (those who have inherited only one copy of the altered gene) are asymptomatic (do not experience symptoms). Two of these altered genes must be present for CF to appear. This means that if both parents are CF carriers, their offspring will express CF symptoms only if the child inherits one defective copy of the CFTR gene from each parent.
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.
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.
Autosomal recessive.
recessive genes!
recessive genes!
If both parents have the gene, the chances are 25% of having a child with Cystic Fibrosis. The male and females x genes are affected by it and only half of it. So when the parents mate and they are going to have a baby, the chances are 25%
What is cystic fibrosis? Cystic fibrosis is a life threatening disease.
cystic fibrosis (:cystic fibrosis :)cystic fibrosis ^-^
Inheritance - Autosomal recessive, requires mutations on both alleles - A single gene on chromosome 7, which encodes for the cystic fibrosis transmembrane conductance regulator - There are over 1000 different mutations for this gene - The most common is Delta F508, which makes up 67% of all mutations in the Caucasian population - Caucasians most effected
Yes, girls can get cystic fibrosis.
Is a carrier of cystic fibrosis
take a genetic test - a blood or tissue sample is analysed for specific mutations