![]() Outcomes and survival rates for cystic fibrosis have improved drastically over the past fifty years. Lack of knowledge about the disease, poor access to health care, confounding diagnoses, a high level of infant mortality in general, and low life expectancy all contribute to the under-diagnosis of the disease. This includes Latin America, Africa, and India. In some parts of the world, cystic fibrosis is under-diagnosed, and the true prevalence of the disease is not known. In Japan, the estimated incidence is 1:100 000 to 1:350 000. In India, the prevalence is estimated at around 1:40 000 to 1:100 000 births. Estimates for the Middle East are between 1:2560 and 1:15,876.Ĭystic fibrosis is rare among Asians. The incidence in Latin America ranges from 1:3900 to 1:8500. In southern Africa, the carrier frequency is 1 in 42, with a calculated incidence of 1 in 7056 births. In Europe, the rate of cystic fibrosis is between 1:2000 and 1:3000 births. Worldwide, the incidence of cystic fibrosis is as high as 1:377 in parts of England and as low as 1:90 000 among Asian people in Hawaii. This is 13 times higher than Asian-American populations, where the prevalence is 1:32 000. who have North European heritage is 1:2500. The birth prevalence among those Caucasian people in the U.S. ![]() The prevalence of cystic fibrosis varies quite a bit between different racial and ethnic groups.
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