Peutz-Jeghers syndrome differential diagnosis: Difference between revisions
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{{CMG}} {{AE}} {{MJK}} | {{CMG}} {{AE}} {{MJK}} | ||
==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]], | 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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[[Category:Genetic disorders]] | [[Category:Genetic disorders]] | ||
[[Category:Syndromes]] | [[Category:Syndromes]] | ||
{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} |
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]
- Cowden syndrome
- Cronkhite-Canada syndrome
- Bannayan–Riley–Ruvalcaba syndrome
- Juvenile polyposis
- Addison's disease
- McCune-Albright syndrome