Paraganglioma epidemiology and demographics: Difference between revisions
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{{Paraganglioma}} | {{Paraganglioma}} | ||
{{CMG}} {{AE}} {{AAM}} | |||
==Overview== | |||
Paraganglioma is a rare disease, familial paragangliomas account for approximately 25% of cases and occur at an earlier age. | |||
==Epidemiology and Demographics== | |||
Familial paragangliomas account for approximately 25% of cases, are often multiple and bilateral, and occur at an earlier age. | |||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
[[Category:Disease]] | [[Category:Disease]] | ||
[[Category:Types of cancer]] | [[Category:Types of cancer]] | ||
[[Category:Mature chapter | [[Category:Mature chapter]] | ||
Revision as of 15:46, 28 August 2015
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Ahmad Al Maradni, M.D. [2]
Overview
Paraganglioma is a rare disease, familial paragangliomas account for approximately 25% of cases and occur at an earlier age.
Epidemiology and Demographics
Familial paragangliomas account for approximately 25% of cases, are often multiple and bilateral, and occur at an earlier age.