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Cystic fibrosis (also known as CF or mucoviscidosis) is an autosomal recessive genetic disorder affecting most critically the lungs, and also the pancreas, liver, and intestine.
Life expectancy development in some big countries of the world since 1960 Life expectancy at birth, measured by region, between 1950 and 2050 Life expectancy by world region, from 1770 to 2018 Human life expectancy is a statistical measure of the estimate of the average remaining years of life at a given age.
People with cystic fibrosis may experience salty skin, persistent coughing, lung infections such as pneumonia and bronchitis, and wheezing and shortness of breath. Cystic fibrosis can also cause poor weight gain and growth, nasal polyps, chronic sinus infections, clubbing or enlargement of fingers and toes, infertility in males, and rectal ...
The average life expectancy, for those affected by CF, is between 42, and 50 years, in the developed world, [7] [8] with lung problems being responsible for roughly 80% of related deaths. [ 1 ] Epidemiology
Cystic fibrosis, the most common life-limiting autosomal recessive disease among people of Northern European heritage Sickle-cell anemia , most prevalent in populations with sub-Saharan African ancestry but also common among Latin-American, Middle Eastern populations, as well as those people of South European regions such as Turkey, Greece, and ...
Cystic fibrosis is the most common life-threatening autosomal recessive disease in the United States and Europe. [28] It is a genetic disorder that affects the lungs, but also the pancreas, liver, kidneys, and intestine. [29] It is caused by mutations in the CFTR protein, a chloride channel expressed in epithelial cells. [28]
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Cystic Fibrosis Worldwide (CFW), [42] an international network concentrated on increasing quality of life and life expectancy for people with cystic fibrosis; CysticFibrosis.com, [43] an internet information hub with support forums