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Doctor insights on: Cystic Fibrosis And Albuterol

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Can you die of cystic fibrosis?

Can you die of cystic fibrosis?

Yes but: Yes but with early diagnosis and regular care and adherence to prescribed therapy by a pediatric pulmonologist the long term survival has improved greatly in the past two decades. ...Read more

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Ventolin (Definition)

Ventolin is the trade name for the chemical / drug albuterol. This drug is a medicine to be inhaled to open the airways and it acts quickly, so it is called a "short-acting bronchodilator". The medicine comes in both a hand-held inhaler and as a liquid to be used with a nebulizer machine. It also comes in a liquid form to take by mouth, but this should not be used ...Read more


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What is risk of cystic fibrosis?

What is risk of cystic fibrosis?

Depends on genes: The risk of acquiring cystic fibrosis (CF) depends on whether the parents of a child are carriers for the gene. It is estimated that about 1 in 20 americans are carriers of the CF gene. In order for a child to acquire the disease, both parents must be carriers. If both parents are carriers, there is then a 25% chance that the child will acquire the disease. ...Read more

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Can you die from cystic fibrosis?

Yes.: Although the complications of cystic fibrosis are treatable, and although the available treatments are helpful, the disorder shortens the normal life expectancy. ...Read more

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What are symptoms of cystic fibrosis?

Cough, poor growth: Common symptoms of cystic fibrosis include cough, wheeze, recurrent lung infections, poor growth, foul smelling stools, salty sweat, clubbing, and rectal prolapse. The more symptoms the greater the chance of having cystic fibrosis. Most infants today are diagnosed by newborn screening for CF before they develop any symptoms and early therapy can minimize disease symptoms. ...Read more

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How to tell if I have cystic fibrosis?

Sweat test: The gold standard to diagnose cystic fibrosis is the sweat test, which measures the amount of chloride in the sweat. The test takes a few minutes to an hour and is painless. It is done in specialized clinics and hospitals. ...Read more

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Conditions that mimic cystic fibrosis?

The list goes on: There are a whole variety of illnesses that can mimic CF from chronic cough, asthma, to immunodeficiency, broncho pulmonary dysphasia celiac disease, Alpha 1-anti trypsin deficiency. ...Read more

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What kind of disease is cystic fibrosis?

What kind of disease is cystic fibrosis?

Genetic: It's a genetic disease that primarily effects the lungs. Here is a great site to learn about cystic fibrosis: http://www. Cff. Org/ ...Read more

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What is cystic fibrosis in children from?

What is cystic fibrosis in children from?

Recessive gene: A mutation is carried in the dna of both unaffected parents & that matching or similar mutation is paired up at conception when the sperm & egg form completed chromasomes with the defective info. Late in pregnancy and after delivery, the effect of the CF gene abnormality begins to reveal itself. In carriers, the good gene compensates for the bad & no problems occur. ...Read more

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Hi what is the cause of cystic fibrosis?

Recessive genes: A mutation is carried in the dna of both unaffected parents ; that matching or similar mutation is paired up at conception when the sperm ; egg form completed chromasomes with the defective info. Late in pregnancy and after delivery, the effect of the CF gene abnormality begins to reveal itself. In carriers, the good gene compensates for the bad ; no problems occur. ...Read more

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What are all the symptoms of cystic fibrosis?

What are all the symptoms of cystic fibrosis?

Respiratory, GI: Mostly respiratory and GI symptoms such as: asthma like symptoms, recurrent pneumonias, lose stool with fawly smell, lipid soluable vitamin deficiencies, diabetes. Shahzeidi, md. ...Read more

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What kind of condition is cystic fibrosis (c.F.)?

Progressive disease: Cystic fibrosis (CF) is a progressive, lifelong condition in which the glands that produce mucus, sweat, and intestinal secretions do not function properly. Thick mucus accumulates in the lungs, leading to breathing difficulty and infection. CF also impairs digestion, and affected males are usually infertile. ...Read more

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What is cystic fibrosis and how can it be treated?

Cystic fibrosis (CF): An inherited condition that affects the cells that produce mucus, sweat and digestive juices. These secreted fluids are normally thin & slippery. But in cf, a defective gene causes the secretions to become thick and sticky. Instead of acting as a lubricant, the secretions plug up tubes, especially in the lungs and pancreas. Treatments are aimed at preventing lung infections & improving nutrition. ...Read more

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If I have cystic fibrosis, could I be an organ doner?

If I have cystic fibrosis, could I be an organ doner?

Organ Donation: Organ donation is possible and should be discussed with Lifelink. Many people do not realize that other useful tissues like heart valves, tendons, corneas are part of the donation process as well and can help recipients. In CF lungs heart, pancreas and liver are likely not able to be shared. See Lifelink http://www. Lifelinkfound. Org/index. Cfm ...Read more

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Help please! Could cystic fibrosis be passed on offspring?

Recessive: Cystic fibrosis (CF) requires both copies of the gene to carry a mutation (one copy each from mother and father). The way a person usually gets CF is if both of their parents are unaffected carriers (one mutated copy and one normal copy). In this situation, there is a 25% chance that the offspring will get cf, 50% chance of being an unaffected carrier, and a 25% of inheriting two normal copies. ...Read more

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Can someone be diagnose with cystic fibrosis in their 40's?

Can someone be diagnose with cystic fibrosis in their 40's?

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

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Should I be concerned about cystic fibrosis? What is cystic fibrosis?

Why?: If you are 45 and have not manifested signs of cystic fibrosis then you don't have it and need not worry. The disease is a genetic defect that requires both genes of the pair to be effected to manifest itself. If you and your partner each carry one defective gene then 25% of your children on average could be affected. See: http://en. Wikipedia. Org/wiki/cystic_fibrosis for more info. ...Read more

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Is cystic fibrosis because of mucus?

Kind of...: Cystic fibrosis (CF) is a genetic disease. Patients with the disease are born with a defective gene that is part of the body's system for making mucus, sweat, and digestive fluids. Their mucus is therefore abnormally thick and causes blockages in the lungs, pancreas and other organs that damage them and make them prone to infections and other problems. ...Read more

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How to tell if I have cystic fibrosis? Is it deadly?

Testing; can be: Cystic fibrosis (CF) can be diagnosed with appropriate examination by a doctor and a sweat chloride testing. No single symptom is unique to that disease. CF can be deadly, at any age, young or old. Severity varies greatly, and lung (respiratory) failure is the most common cause of death from cf. ...Read more

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Dr. Brian Bezack
719 Doctors shared insights

Albuterol (Definition)

Albuterol is a beta 2 agonist that stimulates the muscles in the airways to open up if they are in spasm. Typically the medicine is inhaled via a meter dosed inhaler (mdi), or a nebulizer and also available ...Read more


Dr. William Walsh
988 Doctors shared insights

Cystic Fibrosis (Definition)

A genetic disorder of the lungs and digestive tract. It causes recurrent lung infections and inhibits growth in patients and average life expectancy of patients with cystic fibrosis ...Read more