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it is diagnosed by your parents having a single cf (cistic fibrosis) jean inside of there body so when these two jeans meet they become one witch makes the child have cf this person can be diagnosed at any stage of there life from a few days old to possibly 50 years old.
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Can people with Cystic Fibrosis use hallucinogenic mushrooms?
There is no evidence to show that it will be detremental to the Cistic Fibrosis its self, as long as you maintain your treatment regime there should not be a problem with you using them in moderation.
What if your little sister has cistic fibrosis what should you do?
you should make her feel normal play with but not to much . Go to a doctor . God Bless You And your Family one of these days i will find the cure..........
What type of genetic disorder occurs when the body produces abnormally thick mucus?
Cistic Fibrosis is when Mucus clots up in the lungs and intestines making it harder to breath. =)
Do you need any medical treatment when diagnosed with apical fibrosis in both lungs?
yes or you can die
Your father was diagnosed with idiopathic pulmonary fibrosis What is the prognosis of his life expectancy?
About 5 to 7 years.
How is cystic fibrosis diagnosed?
A medical physician can run a test known as the chloride sweat test that can be used to help diagnose cystic fibrosis. Cystic Fibrosis is a systemic disease that primarily affects the lungs and causes thick mucous secretions to build up in the airway and therefore causes breathing problems.
A six letter word starting with ci and ending with ic?
Citric, cistic
Genetic disorder in which the lungs are clogged with large quantities of abnormally thick mucus?
cistic fiberosis is a desiese that is inherited and effects the lungs and panres it builds up mucus in the lungs this causes infections and thing like broncitis. There is no known cure and the people who have it is only expected to live up to age 40. But it makes it hard to brreath and if you get things like pnmonia it can kill you sooner than the estemated time of death. For more information visit the cistic fibrosis associations website.
How can you detect cystic fibrosis?
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.
What are facts about Cystic Fibrosis?
named for scarring and syst formation in ur pancreas about 1000 people are diagnosed a year this is my school project there is no cure for this yet causes early death is a ressesive trait
Can an Adult get cystic fibrosis?
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.
What is the medical term meaning liver inflammation and fibrosis?
Cirrhosis is defined as liver inflammation and fibrosis. Liver inflammation is hepatitis. Fibrosis is fibrosis.
