Doctor insights on:
How Many People Have Cystic Fibrosis In The World
Yes: The primary symptoms are pulmonary and digestive. Chronic lung disease and recurrent lung infections start early in life. Intestinal malapsortion because of digestive enzyme deficiency also occurs early. Other symptoms include meconium illius in the perinatal period, growth failure in childhood and a variety of symptoms in the second and third decades of life including diabetes. ...Read moreSee 1 more doctor answer
Cystic fibrosis is a genetic disorder involving lungs & digestive tract, causing recurrent lung infections due to thick inspissated mucus & poor growth in majority of patients due to malabsorption. Treatment involves inhaled respiratory therapies to prevent lung disease & pancreatic enzymes to enable absorption of nutrients. Average life expectancy is near 40 years, ...Read more
Try this link.: http://www.cff.org/AboutCF/Get a more detailed answer ›
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 pregnent females are now screened for CF ...Read more
Had holiday gathering with multiple family members and found out that many had cystic fibrosis. What can I do to prevent it?
CF is genetic: 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 moreSee 2 more doctor answers
Depends on Severity: This would depend on the severity of the disease state in the individual, but by and large, it's enough of a difference from "normal" sweat to make one take notice. Clinically, the sweat chloride level is measured twice to make the diagnosis of cystic fibrosis (cf). The cutoff level to make the diagnosis of CF is 60 milliequivalents per liter of sweat chloride. ...Read moreSee 1 more doctor answer
Depends...: There is no way to accurately predict how long a person with cystic fibrosis will live, as many different factors affect a person’s health. Severity of disease and time of diagnosis are two such factors. Many people have a mild case of cf, while others can have moderate or severe. In 2009, the median predicted age of survival was in the mid-30s. ...Read more
Cystic fibrosis: Patients with CF can suffer from sinus, respiratory, pancreatic, and biliary disease. They can also experience infertility, musculoskeletal disease, kidney stones, recurrent venous thrombosis, and small bowel obstruction. Obviously, some of these complications are associated with varying degrees of pain. It is probably more appropriate to ask about the overall morbidity of the disease. ...Read more
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