Cystic Fibrosis : A Disease Essay

1599 Words Nov 23rd, 2015 7 Pages
Cystic Fibrosis is a disease that occurs in chromosome 7 that does not allow children to live normal childhoods due to mucus buildup caused by respiratory deterioration: treatments used for this disease are medication, antibiotics, chest therapy, physical therapy, pulmonary rehabilitation, exercise and good balanced nutrition; however due to the advancement in technology in medication over the past 20 years, healthcare professionals should always treat for cystic fibrosis when the following symptoms are evident such as osteoporosis, liver disease, mental mood swings, difficulty breathing, rapid weight loss, digestive problems and mucus buildup. Cystic Fibrosis occurs in a defective gene on chromosome 7 called CFTR (cystic fibrosis transmembrane conductance regulator). The protein produced by this gene helps salt move in and out of cells; however, if the protein doesn 't work correctly, that movement is blocked and an abnormally thick sticky mucus is produced on the outside of the cell. Lung cells are the ones affected in which case the mucus clogs the airways in the lungs, and increases the risk of infection by bacteria. This disease affects the childhood lives of children who were born with Cystic Fibrosis due to mucus buildup, being one of the main risks in Cystic Fibrosis, as it makes breathing difficult once the lung airways get clogged. Respiratory System complications have various life threatening situations without the proper medication as the child grows.…

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