Difference between revisions of "Cystic fibrosis"

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==Gene==
==Gene==
*CFTR gene.<ref name=omim219700>{{OMIM|219700}}</ref>
*CFTR gene.<ref name=omim219700>{{OMIM|219700}}</ref>
==Clinical features==
Mnemonic ''CF PANCREAS'':<ref>URL: [http://www.valuemd.com/pediatrics_mnemonics.php http://www.valuemd.com/pediatrics_mnemonics.php]. Accessed on: 14 March 2012.</ref>
*Chronic cough.
*Failure to thrive.
*Pancreatic insufficiency, e.g. steatorrhea.
*Alkalosis.
*Nasal polyps & neonatal intestinal obstruction ([[meconium ileus]]).
*[[Clubbing]] & chest x-ray findings.
*Rectal prolapse.
*Electrolyte elevations in sweat.
*Absence of [[vas deferens]].
*Sputum with ''Pseudomonas''.
===Trimmed version===
*PAncreatic insufficiency, e.g. steatorrhea.
*Nasal polyps & neonatal intestinal obstruction ([[meconium ileus]]).
*[[Clubbing]].
*REctal prolapse.
*Absence of [[vas deferens]].
*Sputum with ''Pseudomonas''.


==Associated pathology==
==Associated pathology==
Pulmonary:
Pulmonary:
*[[Bronchiectasis]].
*[[Bronchiectasis]].
*Fibrosis - secondary to infections.


Gastrointestinal tract:
Gastrointestinal tract:
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*[[Meconium ileus]].
*[[Meconium ileus]].
*[[Meconium peritonitis]].
*[[Meconium peritonitis]].
*[[Crohn's disease]].<ref name=pmid8149854>{{Cite journal  | last1 = Lloyd-Still | first1 = JD. | title = Crohn's disease and cystic fibrosis. | journal = Dig Dis Sci | volume = 39 | issue = 4 | pages = 880-5 | month = Apr | year = 1994 | doi =  | PMID = 8149854 }}</ref>


Genitourinary tract:
Genitourinary tract:
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