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Cystic fibrosis : note


Patients with cystic fibrosissecrete very viscous mucus in the lung and
suffer repeated lung infections.The pancreas is also affected and patients
are deficient in pancreaticenzymes; this reduces digestion and absorption
of nutrients, so affecting growth.
The viscous mucus in cysticfibrosis is difficult to clear from the lung:
patients need physical therapy andpostural drainage to clear the airways.
Sweat glands have sympatheticcholinergic innervation. Patients with cystic
fibrosis secrete a large amount ofsalt in their sweat and this forms the basis
of a diagnostic test for thecondition.
Since cystic fibrosis patients lackdigestive enzymes, enzyme preparations
containing amylase, lipase andproteases are prescribed in order to improve
intestinal absorption of nutrients.

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