Doctor insights on:
Integumentary System And Cystic Fibrosis
Cystic Fibrosis: The endocrine system is potentially one of the systems involved in cystic fibrosis. There are many different presentations of cf. If the pancreas is affected then supplements may be needed to help digest food. In addition, some CF patients have a form of diabetes. The cff is a good resource for information. Cff.Org prmg will review your CF records at 858 259 9689 at no cost to you. ...Read more
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
Mucus & infection: The cells lining the airways don't put out enough water into the airway to make airway secretions thin enough to be coughed out. The mucus that collects clog the airways and let germs grow and thrive instead of being killed. Long-term infection damages the airways and substance of the lung. The airways and lung units gradually fill up with pus and germs and can't take in oxygen or get rid of co2. ...Read more
Absolutely: The thicker mucous secretions inherent to cystic fibrosis (CF) can cause a relative obstruction in clearing the airway tree of particulate matter/germs. Similarly, these secretions can obstruct the passage of pancreatic enzymes into the intestine leading to mal-digestion. ...Read moreSee 1 more doctor answer
Varies: Newborns can present with bowel obstruction from lthickened meconium , early stool, from lack of normal enzymes.Sometimes bowel atresia and twisted bowel in utero are other manifestations. In child, respiratory symptoms may result with over aeration and asthmatic symptoms from mucus plugging in lungs. Malabsorption, fatty liver, and anemia in early childhood. Some mild forms do not show until later. ...Read more
Inherited disease: Cystic fibrosis (CF) is an inherited disease that affects the cells lining the lungs, sinuses, intestines, spleen and liver. It prevents chloride ions from crossing the cell membranes properly. This can clog organ ducts. In the lungs, the extra mucus crushes the cilia and leads to more lung infections. Medications can help; in late-stage disease, lung transplantation may be life-saving. ...Read more
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