If both parents are carriers then the child has a 25% chance of having cystic fibrosis.
If one parent has CF and the other the other was just a carrier then the child has a 50% chance of having CF.
If one parent has CF and the other has two normal genes then there is no chance of the child having CF.
If one parent is a carrier and the other has two normal genes then there is no chance of the child having CF.
If both parents have CF then there is a 100% chance that the child will also have CF.
It depends weather or not the woman carries the cystic fibrosis alele. If she carries a recessive CF allele, then the chances of her and the man having a child with CF is 1/4 But if she doesn't carry it then the child wont have CF but could carry the disorder as a recessive allele. again, the chances of that are 1/4.
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.
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%
Zero. Cystic fibrosis is an autosomal recessive disease. This means that both parents must carry a mutated gene and have a 1 in 4 (25%) chance of having a child with CF.
The chances are one half. You will most likley have 2 children without the gene, and 2 with one gene. Since the normal parent has the dominate allele, the Cystic Fiborisis will not be present.
Most babies with cystic fibrosis are diagnosed at birth from meconium ileus (stomach blockage) however if undetected at birth if a doctor is suspicious he can give the "sweat test" which measures the concentration of chloride that is excreted in sweat. for a further list of symptoms here's the cystic fibrosis website in the below related link.
A professional who helps people understand their chances of having a child with a genetic disorder is called a geneticist.
From what I understand there is no such thing as Adult Onset Cystic Fibrosis. CF is a hereditary genetic disease that you are born with. That said, there are rare cases of people with symptoms so mild they were not diagnosed until there 30s-60s. Sometimes these people have had prior medical problems but their doctors didn't check for CF because of their age. It is often so debilitating that children are diagnosed within the first few days of life. I am not an expert, I am just looking for research because I was told to go in for a test today (at age 33). The hospital couldn't even administer the test in the normal lab, I need to go to the children's hospital. I am just now reading http://www.cff.org/ it has more official information.
If you do not have a clear goal in mind, then counseling could definitely assist you in finding a job. If you do have a clear goal then a counselor may be a waist of time.
First resource should be your family physician. They can refer you to a qualified professional. Also, check with your peers. Chances are you are not the only one dealing with this problem!
It can be an issue of consideration in determining the safety of the children.
If the spouse he or she has the gene needed to pass on cystic fibrosis, then yes it will have children with cystic fibrosis. If the spouse does not have that gene then the child will not have cystic fbrosis but will be a gene carrier of cystic fibrosis.