Peutz-Jeghers syndrome risk factors: Difference between revisions
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==Overview== | |||
The most potent risk factor in the development of Peutz-Jeghers syndrome is family history of hamartomatous polyposis syndromes, which include Peutz–Jeghers syndrome, [[juvenile polyposis]], [[Cowden syndrome]], and [[Bannayan–Riley–Ruvalcaba syndrome]]. | |||
== References == | == References == | ||
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[[Category:Genetic disorders]] | [[Category:Genetic disorders]] | ||
[[Category:Syndromes]] | [[Category:Syndromes]] | ||
{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} | ||
Revision as of 17:18, 9 September 2015
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Peutz-Jeghers syndrome Microchapters |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Mohamad Alkateb, MBBCh [2]
Overview
The most potent risk factor in the development of Peutz-Jeghers syndrome is family history of hamartomatous polyposis syndromes, which include Peutz–Jeghers syndrome, juvenile polyposis, Cowden syndrome, and Bannayan–Riley–Ruvalcaba syndrome.