Doctor insights on:
Difference Between Asthma And Cystic Fibrosis
CF vs asthma: There is some overlap. Kids with CF often have other symptoms besides their respiratory ones, like oily stool, failure to gain weight, diarrhea. They can also get frequent bacterial lung infections that children with asthma do not often get. They also tend to produce phlegm that is thicker, white/green and looks more like pus, than the white/clear phlegm that children with asthma produce. ...Read more
Confusing question: Patients with any of the listed conditions can have an infection or infestation by a common pathogen (they can all get strep throat).There is no unifying pathogen that causes all the conditions listed. Perhaps your question is really something else and the words are not quite able to address it. ...Read more
Can u have atypical cystic fibrosis if u have asthma, severe pancreas involvement & CFTR m470v? Report indicates a 2nd gene may be rare or unknown
Maybe: Surprisingly, M470V is a common variation. Studies have shown 50% of the population has this mutation and actually less likely to cause CF. Most individuals with CF and carry M470V have some other hidden etiology that is the cause, rather than M470V. Genetic expression may be variable and so will be the clinical manifestations. Speak with your doc and a geneticist for specific information. ...Read more
I was diagnosed with croup and later with laryngitis. I think I also have cystic fibrosis. How can I tell the difference between the two?
Doubtful: If you suspect you have cystic fibrosis and your doctor thinks further testing is warranted they should be able to order specific testing to rule it out. That being said, croup and laryngitis are not typical presentations of cystic fibrosis. CF symptoms usually present much earlier than age 20 yrs. ...Read more
Meconium: Meconium is the poo you make in the womb but are not supposed to empty until after birth. It represents bile/swallowed hair & skin cells etc & is very sticky. If you poo before birth, usually due to stress, the stuff can circulate in the bag of waters. If that material gets into your lungs before, during or after labor it can cause lung disease. CF kids have poo that's too sticky & won't pass. ...Read more
Different mutations: Mutations in the cftr gene cause cystic fibrosis. The cftr gene provides instructions for making a channel that transports negatively charged particles called chloride ions into and out of cells. More than 1, 000 different mutations in the cftr gene have been identified in people with cystic fibrosis. Depending on the which mutations and other genetic factors, this leads to variability of disease. ...Read more
Certainly: Cystic Fibrosis (CF) most common life-limiting genetic disorder of Caucasians, affecting approximately 30K people in the US. A, impacting mainly respiratory function. In recent years patients symptoms better controlled by genetic findings and better medications. Emotional & phys. Development depend on severity, time in hospital, complications. Morb. & mort. Factors afect emotional, cognitive behavior. ...Read more
I want to see if there's any additional therapy I can do for my boyfriend. He has cystic fibrosis and I'd like to try to help ease the symptoms.
CF center: First I wish him all the best and good health and thank you for caring for him, any cystic fibrosis patient should be followed by specialists in a cystic fibrosis center, if you haven't done that already, please check the cystic fibrosis foundation on the web for help, www. Cff. Org, goodluck ...Read more
As a carrier:
Genetic carrier testing:
more than 10 million americans are symptomless carriers of the defective CF gene. This blood test can help detect carriers, who could pass CF onto their children. To have cystic fibrosis, a child must inherit one copy of the defective CF gene from each parent. ...Read more
What are the chances of a child getting cystic fibrosis among the different racial groups in the u.S.?
Acording to the CF foundation: the overall birth prevalence is 1/3700. It can occur in any race, however the greatest incidence is in caucasians of northern european descent, being 1/2500. The other major groups affected are hispanics 1/13500, african americans 1/15000.
More than 10 million of us carry one part of the defective gene, but to have the disease you must have a copy from both parents. ...Read more
Equal: More than 10 million americans are unknowing, symptomless carriers of the defective cystic fibrosis gene. In order to develop cf, an individual must inherit a defective gene from each parent. Since the CF gene is not on a sex chromosome (x or y), males and females are equally affected. ...Read more
Not specifically: Most CF patients that are monitored and receiving regular healthcare can not be picked out in a crowd of people of similar age. If their disease were to go unrecognized and or untreated they would appear ill. ...Read more
Sweat chloride test: CF is an abnormality of chloride channels. A simple test where they tape a special paper to your arm and measure the amount of chloride in your sweat can help rule in or out cf. ...Read more
Depends on ethnicity: CF is a genetic condition inherited from carrier parent. Carrier frequency depends on the ethnic background. 1/25 caucasians have one copy of normal, one copy of a mutated CF gene. Both genes have to be mutated to have cf. Hispanic carrier frequency 1/50, africanam 1/70, Asian 1/90. 1/5000 babies are born with cf, this may be decreasing, since pregnant females are now screened for CF ...Read more
I can't think of any: As above.Get a more detailed answer ›
Cystic fibrosis: Early diagnosis and management with likely increase your live expectancy. ...Read more
Varies: Unfortunately, there is no correct answer to this. It really varies and depends on various factors, including the type of mutation a patient may have. Symptoms may start soon after birth, or years later. ...Read more
Genetic disease: CF is a genetic disease caused by an absence or a defect in the protein that moves sodium and chloride in and out of pit helical cells. This leads to thick mucus in several areas, particularly the pancrease (pancrelipase), (pancrelipase) lungs, and gut. In the lungs, the mucus itself leads to obstruction and can become chronically infected, the pancrease (pancrelipase) and gut can become clogged, leading to failure of the pancrease (pancrelipase). ...Read more
Genetic illness: It is a genetic illness that affects the mucus in the lung and the pancreas, leading to progressive lung function decline and pancreatic insufficiency. It is usually diagnosed at birth with standard screening tests. Prior to birth, both parents can have genetic testing to assess their risk of having a child with cf. ...Read more
It depends: It really depends on the severity of the disease. Not all patients experience the same symptoms and the same course. ...Read more
Varies considerably: There is considerable variance between children and between institutions for the cost of of hospitalizing a child with cf. Children have variable needs for hospitalization depending on their genotype and adherence to their regimen, and (unfortunately) there is a large amount of variance in practices while hospitalized and costs for these practices. ...Read more
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