Doctor insights on:
What Is The Karyotype Of Someone With Cystic Fibrosis
Variable: This depends on the individual patient. There are several hundred CF mutations that have varying degrees of severity. The most common mutation, df508, can cause failure to thrive in infants, recurrent and very serious lung infections during childhood and often pancreatic insufficiency in children. While early diagnosis and preventive treatment have improved, CF is still a fatal disease. ...Read moreSee 1 more doctor answer
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 moreSee 1 more doctor answer
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 moreSee 1 more doctor answer
CF is recessive: Cystic fibrosis is a disorder passed thru the genes of both parents, silent in the carrier parent & expressed in the affected kid who has inherited an affected gene from both parents.One mutation(delta 509) is the most common but others occur and variations in intensity do occur. I believe you can have carrier testing to see if u carry a gene, then avoid a starting a pregnancy with another carrier. ...Read more
Usually good: In women with cystic fibrosis, vaginal mucus is often thicker, making it more difficult for the sperm to travel and for fertilization to take place. It often takes longer for women with cystic fibrosis to become pregnant, although this in no way affects the pregnancy itself or the fetus (85% of couples conceive within the first 12 months after stopping contraception). Ivf is also an option. ...Read more
CF diet/supplements: The caloric needs of a CF patient can be 20-30% higher or more than someone without cf. The use of calories for example in respiratory effort uses calories that would otherwise not be expended. Eating a high protein high calorie diet along with CF nutritional supplements will help boost caloric intake. I hope that this helps. ...Read more
Nutrition/prevention: Cystic fibrosis treatment plans depend on the clinical, infectious and gene mutation. There are some treatments delivered by inhalation to thin airway secretions and others to treat or prevent infections. Growth charts will monitor that growth of the baby and supplements may be provided to boost calories. I hope that this helps. Prmg pediatrics can review records faxed to 858 259 9689. ...Read moreSee 1 more doctor answer
Depends on Both: This depends on whether both parents carry the trait. If only one parent is a carrier of the gene, then there is no chance of inheriting cystic fibrosis. However, if both parents carry the CF gene, then there is a 25% chance their child will inherit cystic fibrosis. ...Read moreSee 1 more doctor answer
Anything: Most individuals with cystic fibrosis can participate in all physicial activities. Salt supplementation is needed because of excess salt loss in CF sweat. Individuals with severe lung disease should discuss what level of activity is safe/appropriate for them with their physician. ...Read more
Not very close!: Good morning, patients with cystic fibrosis have many difficulties due to recurrent infections and many visits to doctors. Things have changed recently with an aggressive treatment approach provided centers with specialty clinics for management of cf., yet it will far from being close to having a life similar to one without cf. Follow the instructions of the team for the best possible quality. ...Read more
Depends on Lung Fx: The level of physical activity for a child with CF is an individual choice that should be made in consultation with the treating physician. However, there has been some interesting research done in australia, which suggests Hypertonic Saline (e.g., salty air) inhalation in CF patients was beneficial in maintaining lung function. Why? A doctor noticed surfers with CF tend to have better outcomes! ...Read moreSee 1 more doctor answer
Would it be recommendable for someone with cystic fibrosis to breathe salt vapor in/at the salt room in orlando, fl.?
Good question...: While the process itself may be helpful in mobilizing secretions, i personally would be a bit hesitant to do this type of therapy in a public forum. You really don't know how sanitary they really are (they may tell you one thing, but..), and i'd be very concerned about the types of germs that could lurk in that type of large establishment. Can you find out anything about inspections/health code? ...Read more
Averages: At one year 90 percent of CF patients are alive after lung transplant; the number falls to around 60% at 5 years and 10-15% at 10 years. Double lung transplant patients tend to do better than single lung transplant recipients (probably because they have more reserve if they develop rejection). ...Read moreSee 2 more doctor answers
Yes: Lung transplantation is a very important treatment option for people with cystic fibrosis that is severely limiting their physical ability. If successful, and it usually is, lung transplantation can offer a person with cystic fibrosis a renewed chance to regain the ability and energy to do many activities that others without this condition take for granted, including some sports. ...Read moreSee 2 more doctor answers
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
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
Yes: Yes it is possible. Presentation of cystic fibrosis varies greatly, and it is possible, depending on your specific mutation (and other factors) to present at a later age. In order to prevent late diagnoses, all states now have a newborn screen in place for cystic fibrosis. ...Read moreSee 1 more doctor answer
Not necessarily: I've never met anyone who could.Get a more detailed answer ›
I have family members with cystic fibrosis. Is it possible to start show the symptoms in my 20's?
What are the chances of a child getting cystic fibrosis among the different racial groups in the u.S.?
Overall 1/3700: 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 moreSee 1 more doctor answer
Yes, they CAN, but: Addison's disease has been associated with other autoimmune glandular disorders, including malabsorption and type i diabetes. But cf, although having pancreatic (including diabetes i) & GI deficiencies (malabsorption), is a chromosomal not autoimmune disorder. Their association would be purely coincidental. See: neufeld, m, et al. Medicine: september 1981 - volume 60 - issue 5 - ppg 355-362. ...Read more
Genetic disorder: It is a genetic disorder characterized by abnormal sodium channels, which affect a great deal of problems including the respiratory and digestive systems. It is most commonly diagnosed in infants failing to gain appropriate weight, and in children who have multiple chronic infections. ...Read moreSee 1 more doctor answer
Inherited disease: Cystic fibrosis (CF) is an inherited disease that affects the cells lining the lungs, sinuses, intestines, spleen and liver. It prevents chloride ions from crossing the cell membranes properly. This can clog organ ducts. In the lungs, the extra mucus crushes the cilia and leads to more lung infections. Medications can help; in late-stage disease, lung transplantation may be life-saving. ...Read more
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