10 Facts about Cystic Fibrosis
The genetic disorder primarily affecting the lung is explained on Facts about Cystic Fibrosis. This health condition can spread into the intestine, kidneys, liver and pancreas. Due to the severe lung infection, the patient of Cystic Fibrosis experiences difficulty to breath. The symptoms experienced by the patient depend on how severe the condition is. Let me show you some facts about Cystic Fibrosis below:
Facts about Cystic Fibrosis 1: the general symptoms of Cystic Fibrosis
There are several symptoms of Cystic Fibrosis. Those include clubbing on the fingers, poor growth, coughing up mucus, sinus infections, infertility in males, clubbing on toes, and fatty stool.
Facts about Cystic Fibrosis 2: the cause
The patient is diagnosed with Cystic Fibrosis because of the genetic mutation on CFTR protein. CFTR stands for cystic fibrosis transmembrane conductance regulator. Find facts about coughing here.
Facts about Cystic Fibrosis 3: the function of CFTR
CFTR protein is very important in human body. It is responsible for the mucus, digestive fluid and sweat production.
Facts about Cystic Fibrosis 4: the non functional CFTR
The secretion of CFTR will be thicker when it is not functional. The genetic testing and sweat test can be conducted to diagnose it.
Facts about Cystic Fibrosis 5: the cure
Cystic Fibrosis cannot be cured. Since it is always associated with infection, the physician will prescribe antibiotic to reduce the pain. Find facts about childhood cancer here.
Facts about Cystic Fibrosis 6: the lung transplantation
The patient will be recommended by the physician to have lung transplantation if the infection on the lung is severe.
Facts about Cystic Fibrosis 7: the life expectancy
The patients with Cystic Fibrosis who live in the developing world are expected to live around 42 to 50 years.
Facts about Cystic Fibrosis 8: the death
Most patients with Cystic Fibrosis pass away because of the lung infection. It is found in 80 percent of the death cases.
Facts about Cystic Fibrosis 9: the ancestry
The risk for the people with Northern European ancestry to have Cystic Fibrosis is higher. The genetic disorder is less common in Asian and African ancestry. In 1938, Dorothy Andersen recognized Cystic Fibrosis for the first time.
Facts about Cystic Fibrosis 10: infertility
The men and women who have Cystic Fibrosis have to deal with infertility risk. The reports state that around 97 percent of males with Cystic Fibrosis are infertile. If they want to have kids, the assisted reproductive methods can be conducted since they are not sterile.
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