Cystic fibrosis - Revision history

Michael: wikify

2022-01-31T18:11:59Z

wikify

← Older revision		Revision as of 18:11, 31 January 2022
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	*Alkalosis.		*Alkalosis.
	*Nasal polyps & neonatal intestinal obstruction ([[meconium ileus]]).		*Nasal polyps & neonatal intestinal obstruction ([[meconium ileus]]).
	*Clubbing & chest x-ray findings.		*[[Clubbing]] & chest x-ray findings.
	*Rectal prolapse.		*Rectal prolapse.
	*Electrolyte elevations in sweat.		*Electrolyte elevations in sweat.
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	*PAncreatic insufficiency, e.g. steatorrhea.		*PAncreatic insufficiency, e.g. steatorrhea.
	*Nasal polyps & neonatal intestinal obstruction ([[meconium ileus]]).		*Nasal polyps & neonatal intestinal obstruction ([[meconium ileus]]).
	*Clubbing.		*[[Clubbing]].
	*REctal prolapse.		*REctal prolapse.
	*Absence of [[vas deferens]].		*Absence of [[vas deferens]].

Michael: /* Associated pathology */

2014-09-04T17:52:13Z

Associated pathology

← Older revision		Revision as of 17:52, 4 September 2014
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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:

Michael: /* Clinical features */

2012-05-05T04:58:33Z

Clinical features

← Older revision		Revision as of 04:58, 5 May 2012
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	*Rectal prolapse.		*Rectal prolapse.
	*Electrolyte elevations in sweat.		*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]].		*Absence of [[vas deferens]].
	*Sputum with ''Pseudomonas''.		*Sputum with ''Pseudomonas''.

Michael: /* Associated pathology */

2012-05-05T04:52:11Z

Associated pathology

← Older revision		Revision as of 04:52, 5 May 2012
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	Pulmonary:		Pulmonary:
	*[[Bronchiectasis]].		*[[Bronchiectasis]].
			*Fibrosis - secondary to infections.

	Gastrointestinal tract:		Gastrointestinal tract:

Michael: more

2012-03-14T23:44:39Z

← Older revision		Revision as of 23:44, 14 March 2012
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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''.

	==Associated pathology==		==Associated pathology==

Michael: +dx ca.t

2012-02-28T02:53:29Z

+dx ca.t

← Older revision		Revision as of 02:53, 28 February 2012
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	[[Category:Pediatric pathology]]		[[Category:Pediatric pathology]]
			[[Category:Diagnosis]]

Michael: /* References */

2012-02-28T02:52:42Z

References

← Older revision		Revision as of 02:52, 28 February 2012
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	{{Reflist\|2}}		{{Reflist\|2}}

	[[Category:~~Stuff~~]]		[[Category:Pediatric pathology]]

Michael: fix ref.

2012-02-28T02:50:45Z

fix ref.

← Older revision		Revision as of 02:50, 28 February 2012
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	==Gene==		==Gene==
	*CFTR gene.<ref name=omim219700>{{~~omim~~\|219700}}</ref>		*CFTR gene.<ref name=omim219700>{{OMIM\|219700}}</ref>

	==Associated pathology==		==Associated pathology==

Michael: create

2012-02-28T02:50:18Z

create

New page

'''Cystic fibrosis''', abbreviated '''CF''', a genetic disease that predominantly affects the lungs. It is inherited autosomal recessive.

==Gene==
*CFTR gene.<ref name=omim219700>{{omim|219700}}</ref>

==Associated pathology==
Pulmonary:
*[[Bronchiectasis]].

Gastrointestinal tract:
*Pancreatic insufficiency.
*[[Meconium ileus]].
*[[Meconium peritonitis]].

Genitourinary tract:
*Infertility - bilateral absence [[vas deferens]].<ref name=pmid11035677>{{Cite journal | last1 = McCallum | first1 = TJ. | last2 = Milunsky | first2 = JM. | last3 = Cunningham | first3 = DL. | last4 = Harris | first4 = DH. | last5 = Maher | first5 = TA. | last6 = Oates | first6 = RD. | title = Fertility in men with cystic fibrosis: an update on current surgical practices and outcomes. | journal = Chest | volume = 118 | issue = 4 | pages = 1059-62 | month = Oct | year = 2000 | doi = | PMID = 11035677 }}</ref>

==See also==
*[[Lung]].
*[[Pediatric pathology]].

==References==
{{Reflist|2}}

[[Category:Stuff]]