Cystic fibrosis natural history, complications and prognosis: Difference between revisions
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==Prognosis== | ==Prognosis== | ||
Life expectancy of patients with the disorder has been greatly increased over past decades because of better notions of symptomatic treatment strategies. | |||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
[[Category:Gastroenterology]] | [[Category:Gastroenterology]] |
Revision as of 21:04, 8 February 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief:
Overview
If left untreated, [#]% of patients with [disease name] may progress to develop [manifestation 1], [manifestation 2], and [manifestation 3].
OR
Common complications of [disease name] include [complication 1], [complication 2], and [complication 3].
OR
Prognosis is generally excellent/good/poor, and the 1/5/10-year mortality/survival rate of patients with [disease name] is approximately [#]%.
Natural History, Complications, and Prognosis
Natural History
Complications
Prognosis
Life expectancy of patients with the disorder has been greatly increased over past decades because of better notions of symptomatic treatment strategies.