Peutz-Jeghers syndrome risk factors: Difference between revisions

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{{Peutz-Jeghers syndrome}}
{{Peutz-Jeghers syndrome}}
{{CMG}} {{AE}} {{MJK}}
{{CMG}} {{AE}} {{HQ}}
==Overview==
==Overview==
Common risk factor in the development of Peutz-Jeghers syndrome is the presence of [[family history]] of Peutz-Jeghers syndrome.
Common risk factor in the development of Peutz-Jeghers syndrome is the presence of [[family history]] of Peutz-Jeghers syndrome.
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== References ==
== References ==
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{{reflist|2}}
{{Phakomatoses}}
{{Digestive system neoplasia}}
[[Category:Dental disorders]]
[[Category:Gastroenterology]]
[[Category:Genetic disorders]]
[[Category:Syndromes]]
{{WH}}
{{WS}}
[[Category:Up-To-Date]]
[[Category:Oncology]]
[[Category:Medicine]]
[[Category:Gastroenterology]]
[[Category:Surgery]]

Revision as of 13:13, 18 December 2017

Peutz-Jeghers syndrome Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Hamid Qazi, MD, BSc [2]

Overview

Common risk factor in the development of Peutz-Jeghers syndrome is the presence of family history of Peutz-Jeghers syndrome.

Common Risk Factors

Common risk factor in the development of Peutz-Jeghers syndrome is the presence of family history of Peutz-Jeghers syndrome.


References