Peutz-Jeghers syndrome differential diagnosis: Difference between revisions

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==Overview==
==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]].
Peutz-Jeghers syndrome must be differentiated from other diseases that cause [[hamartomatous]] [[polyps]] and mucocutaneous pigmentation, such as [[Cowden syndrome]], [[Bannayan–Riley–Ruvalcaba syndrome]], [[juvenile polyposis]], [[Addison's disease]], and [[McCune-Albright syndrome]].


==Differentiating Peutz-Jeghers Syndrome from other Diseases==
==Differentiating Peutz-Jeghers Syndrome from other Diseases==
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Revision as of 15:20, 18 September 2015

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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

Peutz-Jeghers syndrome must be differentiated from other diseases that cause hamartomatous polyps and mucocutaneous pigmentation, such as Cowden syndrome, Bannayan–Riley–Ruvalcaba syndrome, juvenile polyposis, Addison's disease, and McCune-Albright syndrome.

Differentiating Peutz-Jeghers Syndrome from other Diseases

Peutz-Jeghers syndrome must be differentiated from the following diseases:[1]

References

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