Cystic fibrosis: Difference between revisions
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==Background== | ==Background== | ||
*Autosomal recessive genetic disorder that occurs due to a mutation in cystic fibrosis transmembrane conductance regulator protein or CTFR, which is a chloride channel that is essential to the function of mucus and sweat. Patient's with cystic fibrosis do not have CTFR, therefore are unable to produce the essential components of digestive fluids, mucus, and sweat. Therefore the most common problem that these patients have are diseases related to the lung ([[pneumonia]], [[bronchiectasis]]) and GI tract ([[pancreatitis]]). | |||
==Clinical Features== | |||
==Differential Diagnosis== | |||
==Evaluation== | |||
==Management== | |||
==Disposition== | |||
==See Also== | |||
==External Links== | |||
==References== | |||
<references/> | |||
[[Category:Pulmonary]] | |||
Revision as of 22:06, 1 September 2016
Background
- Autosomal recessive genetic disorder that occurs due to a mutation in cystic fibrosis transmembrane conductance regulator protein or CTFR, which is a chloride channel that is essential to the function of mucus and sweat. Patient's with cystic fibrosis do not have CTFR, therefore are unable to produce the essential components of digestive fluids, mucus, and sweat. Therefore the most common problem that these patients have are diseases related to the lung (pneumonia, bronchiectasis) and GI tract (pancreatitis).