Peutz-Jeghers syndrome differential diagnosis: Difference between revisions
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{{Peutz-Jeghers syndrome}} | {{Peutz-Jeghers syndrome}} | ||
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==Overview== | |||
Peutz-Jeghers syndrome must be differentiated from other diseases that cause hamartomatous polyps and mucocutaneous pigmentation, such as [[Cowden syndrome]], [[Bannayan–Riley–Ruvalcaba syndrome]], and [[juvenile polyposis]]. | |||
== References == | == References == | ||
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[[Category:Syndromes]] | [[Category:Syndromes]] | ||
[[Category:Needs content]] | [[Category:Needs content]] | ||
{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} | ||
Revision as of 15:10, 9 September 2015
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Peutz-Jeghers syndrome Microchapters |
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Diagnosis |
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Peutz-Jeghers syndrome differential diagnosis On the Web |
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Risk calculators and risk factors for Peutz-Jeghers syndrome differential diagnosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Mohamad Alkateb, MBBCh [2]
Overview
Peutz-Jeghers syndrome must be differentiated from other diseases that cause hamartomatous polyps and mucocutaneous pigmentation, such as Cowden syndrome, Bannayan–Riley–Ruvalcaba syndrome, and juvenile polyposis.