Doctor insights on:
Cystic Fibrosis Complete
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
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
CF and environment: Depending on the severity of your cf, leading an active healthy lifestyle outside is not a fantasy. Common sense will dictate avoidance germs by simple hand hygiene (wash, wipe, alcohol base hand gels). Knowing your CF treatment plan as per your pulmonologist/specialist is important for slowing down the progression/maintaining a more resilient defense against bacterial/chronic lung infection. ...Read more
Genetic: CF is caused by mutations in the cftr gene - mostly they are inhereted from both the mother and father who are carriers (but rarely these mutations can occur spontaneously). Club feet can be caused by several circumstances - some from a generic defect, some from problems during fetal deveopment or toxic exposures. ...Read more
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
Short answer is yes.:
Episodes of joint pain are well recognised in cystic fibrosis (CF), usually starting after ten years of age, and occurring in about five to ten percent of patients (Lawrence et al, 1993).
Continue with this link:
http://www.cfmedicine.com/htmldocs/CFText/arthritis.htm ...Read more
Check: Out cff.Org.Get a more detailed answer ›
One gene bad: The cftr gene codes for (has information for your body about) a sodium-chloride transporter on your cell membranes. If you have two bad copies you have cf, if you have one, you are a carrier. As many as 1 in 25 caucasian adults in the us has this mutation. If you are planning on having children, talk to your spouse about genetic counseling, unless your spouse is of Asian or african descent. ...Read more
My son & wife tested neg for Cystic Fibrosis through screening test, not sweat test. However my son has hirschsprung disease. Should I test for CF - or it's high unlikely I have it? I'm 32. Feel fine
I wouldn't: There is no relationship between Hirschprung disease and CF. If you wand to know if you are an asymptomatic carrier of CF, the tests are available. However, you don't get to age 30 without symptoms when you have the disease and your fertility would also be diminished.If your wife is not a carrier, you can not produce babies with CF. ...Read more
Cystic fibrosis and percentage of lung that still functions properly? How low does it need to be to qualify for a transplant?
Around 30 %: Many things about a patient and their cystic fibrosis (CF) are considered when a team is deciding whether or not to do a lung transplant. When lung function gets bad enough that the patient might die with a bad flare up or infection (often near 30%), they may be listed to get new lungs. It usually takes months to get new lungs, so teams want to use that time to improve strength and nutrition. ...Read more
No: Not every day is bad with cystic fibrosis! the severity of the disease varies from patient to patient. Some patient may not feel they have anything wrong with them. Others may experience breathing difficulties or other symptoms, for example abdominal discomfort. Patients with CF often are required to take numerous medications a day and receive numerous breathing treatments as well. ...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
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
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.?
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
Get tested: Testing for cystic fibrosis starts with a sweat test. If that is abnormal, genetic testing in the blood is used to confirm the diagnosis by finding the specific genetic mutations. In general, people with CF have recurrent pulmonary infections and abdominal discomfort/diarrhea due to fat malabsorption. ...Read more
Cystic fibrosis is a risk factor for:: Aspergillosis, Brain abscess, Bronchiectasis, Collapsed lung, Hypertriglyceridemia, Pulmonary Aspergillosis, Sinusitis, Mucocele, Sputum, Phlegm, Rectal prolapse, Acute sinusitis, Vitamin A deficiency, Vitamin K deficiency, Vitamin E deficiency, Vitamin D deficiency. ...Read more