Cystic fibrosis laboratory findings: Difference between revisions
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{{Cystic fibrosis}} | {{Cystic fibrosis}} | ||
{{CMG}}; {{AE}} {{SHH}} | |||
==Overview== | ==Overview== | ||
[[Immunoreactive trypsinogen]] (IRT) of [[serum]] is raised in newborns with cystic fibrosis and has been used as a [[Screening (medicine)|screening test]]. Also [[Iron deficiency anemia]] is common in patients with cystic fibrosis. | |||
==Laboratory Findings== | ==Laboratory Findings== | ||
* [[Immunoreactive trypsinogen]] (IRT) of [[serum]] is raised in newborns with cystic fibrosis and has been used as a [[Screening (medicine)|screening test]].<ref name="pmid2704582">{{cite journal |vauthors=Rock MJ, Mischler EH, Farrell PM, Bruns WT, Hassemer DJ, Laessig RH |title=Immunoreactive trypsinogen screening for cystic fibrosis: characterization of infants with a false-positive screening test |journal=Pediatr. Pulmonol. |volume=6 |issue=1 |pages=42–8 |date= 1989 |pmid=2704582 |doi= |url=}}</ref> | |||
* [[Complete blood count|'''Complete blood count''']]''':''' [[Iron deficiency anemia]] is common in patients with cystic fibrosis and can be related to GI problems and chronic [[inflammation]].<ref name="pmid11796431">{{cite journal |vauthors=Reid DW, Withers NJ, Francis L, Wilson JW, Kotsimbos TC |title=Iron deficiency in cystic fibrosis: relationship to lung disease severity and chronic Pseudomonas aeruginosa infection |journal=Chest |volume=121 |issue=1 |pages=48–54 |date=January 2002 |pmid=11796431 |doi= |url=}}</ref> | |||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
[[Category: | {{WH}} | ||
[[Category: | {{WS}} | ||
[[Category:Medicine]] | |||
[[Category:Up-To-Date]] | |||
[[Category:Gastroenterology]] | [[Category:Gastroenterology]] | ||
[[Category:Pediatrics]] | [[Category:Pediatrics]] | ||
[[Category:Pulmonology]] | [[Category:Pulmonology]] | ||
Latest revision as of 20:39, 29 March 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Shaghayegh Habibi, M.D.[2]
Overview
Immunoreactive trypsinogen (IRT) of serum is raised in newborns with cystic fibrosis and has been used as a screening test. Also Iron deficiency anemia is common in patients with cystic fibrosis.
Laboratory Findings
- Immunoreactive trypsinogen (IRT) of serum is raised in newborns with cystic fibrosis and has been used as a screening test.[1]
- Complete blood count: Iron deficiency anemia is common in patients with cystic fibrosis and can be related to GI problems and chronic inflammation.[2]
References
- ↑ Rock MJ, Mischler EH, Farrell PM, Bruns WT, Hassemer DJ, Laessig RH (1989). "Immunoreactive trypsinogen screening for cystic fibrosis: characterization of infants with a false-positive screening test". Pediatr. Pulmonol. 6 (1): 42–8. PMID 2704582.
- ↑ Reid DW, Withers NJ, Francis L, Wilson JW, Kotsimbos TC (January 2002). "Iron deficiency in cystic fibrosis: relationship to lung disease severity and chronic Pseudomonas aeruginosa infection". Chest. 121 (1): 48–54. PMID 11796431.