- What race is cystic fibrosis most common in?
- How old is the oldest living person with cystic fibrosis?
- Can a child have CF if only one parent is a carrier?
- Can a black person have cystic fibrosis?
- Is CF curable?
- What gender is cystic fibrosis most common in?
- Can cystic fibrosis go undetected?
- How do I know if my child has CF?
- Can you have CF and not know?
- How is CF inherited?
- Can a child have cystic fibrosis if neither parent has it?
- Can you get cystic fibrosis later in life?
- How does cystic fibrosis affect you sexually?
- What is the life expectancy of cystic fibrosis?
- Does CF run in families?
- How common is it to be a CF carrier?
- How is cystic fibrosis transmitted?
- Can you kiss someone with cystic fibrosis?
What race is cystic fibrosis most common in?
Cystic fibrosis is a common genetic disease within the white population in the United States.
The disease occurs in 1 in 2,500 to 3,500 white newborns.
Cystic fibrosis is less common in other ethnic groups, affecting about 1 in 17,000 African Americans and 1 in 31,000 Asian Americans..
How old is the oldest living person with cystic fibrosis?
The oldest person diagnosed with CF for the first time in the U.S. was 82, in Ireland was 76, and in the United Kingdom was 79. Those diagnosed after age 50 tend to have a long history of frequent bouts of colds, sinus infections, pneumonia, stomach pains, acid reflux, and trouble gaining or keeping on weight.
Can a child have CF if only one parent is a carrier?
If only one parent is a carrier of a defective CF gene, the child will not have CF. But there is a 50% (1-in-2) chance that the child will be a CF carrier. If both parents are carriers, there is a 25% (1-in-4) chance that the child will have CF, and a 50% chance that the child will be a carrier.
Can a black person have cystic fibrosis?
Although CF is a common autosomal recessive disorder in populations of European descent, it is relatively rare in the African-American population (1 in 17,000), with only Asian population ancestries being less affected than African blacks.
Is CF curable?
Treatments for cystic fibrosis. There’s no cure for cystic fibrosis, but a range of treatments can help control the symptoms, prevent or reduce complications, and make the condition easier to live with. Regular appointments to monitor the condition are needed and a care plan will be set up based on the person’s needs.
What gender is cystic fibrosis most common in?
Summary: Researchers have discovered why females with cystic fibrosis do worse than males. The study is the first to show that the female hormone estrogen promotes the presence of a particular form of bacteria which results in more severe symptoms for female cystic fibrosis patients.
Can cystic fibrosis go undetected?
Some people with cystic fibrosis were diagnosed as babies, while others are not diagnosed until they are older. If the disease is mild at first, a person with cystic fibrosis may not experience problems until reaching his or her teen years – or even adulthood.
How do I know if my child has CF?
Signs and symptoms of CF include: Coughing, wheezing or shortness of breath or having a lot of mucus in the lungs or lung infections, like pneumonia and bronchitis. Salty skin. Stuffy nose, sinus infections or nasal polyps (small growths of tissue inside the nose)
Can you have CF and not know?
While cystic fibrosis is usually diagnosed in childhood, adults with no symptoms (or mild symptoms) during their youth can still be found to have the disease.
How is CF inherited?
Every person inherits two CFTR genes, one gene from each parent. Children who inherit a CFTR gene with a mutation from both parents will have cystic fibrosis. When a mutated CFTR gene is inherited from only one parent and a normal CFTR gene is inherited from the other, the person will be a cystic fibrosis carrier.
Can a child have cystic fibrosis if neither parent has it?
Can my children have CF even if it is not in my family? Yes. In fact, most couples who have a child with CF have no family history of cystic fibrosis and are surprised to learn that they carry a mutation in the CFTR gene, which causes the condition.
Can you get cystic fibrosis later in life?
As with other genetic conditions, cystic fibrosis will have been present since birth, even if it is diagnosed later in life. One in 25 people carry the faulty gene that causes cystic fibrosis. To have cystic fibrosis, both parents must be carriers of the faulty cystic fibrosis gene.
How does cystic fibrosis affect you sexually?
Adults with CF have normal levels of sex hormones (progesterone, estrogen, and testosterone) and can lead normal sex lives, as the sexual performance or desire for intimacy is not affected. However, people with CF have thick mucus which can affect fertility.
What is the life expectancy of cystic fibrosis?
Outlook (Prognosis) Many young adults with CF finish college or find jobs. Lung disease eventually worsens to the point where the person is disabled. Today, the average life span for people with CF who live to adulthood is about 44 years. Death is most often caused by lung complications.
Does CF run in families?
Cystic fibrosis (CF) is a genetic, or inherited, disease that occurs when both parents pass a CF gene on to their child. Cystic fibrosis can be found in all races and ethnic groups.
How common is it to be a CF carrier?
It is estimated that approximately 1 in 35 Americans is a carrier of the CFTR gene mutation, which means more than 10 million Americans are cystic fibrosis carriers.
How is cystic fibrosis transmitted?
Cystic Fibrosis is transmitted in an autosomal resave manner. Both parents must have the defective gene and pass it to their offspring to have a child with cystic fibrosis.
Can you kiss someone with cystic fibrosis?
People with CF can’t be together. As a result, people with CF harbor dangerous bacteria in their lungs and these bacteria are contagious only to other people with CF or compromised immune systems.