Peutz-Jeghers syndrome risk factors: Difference between revisions
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{{CMG}} {{AE}} {{MJK}} | {{CMG}} {{AE}} {{MJK}} | ||
==Overview== | ==Overview== | ||
Common risk factors in the development of Peutz-Jeghers syndrome are mutation in ''[[STK11]]'' (''LKB1'') gene and family history of Peutz-Jeghers syndrome. | |||
==Common Risk Factors== | |||
Common risk factors in the development of Peutz-Jeghers syndrome are: | |||
*''[[STK11]]'' (''LKB1'') [[gene mutation]] | |||
*[[Family history]] of Peutz-Jeghers syndrome | |||
== References == | == References == | ||
Revision as of 17:35, 9 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
Common risk factors in the development of Peutz-Jeghers syndrome are mutation in STK11 (LKB1) gene and family history of Peutz-Jeghers syndrome.
Common Risk Factors
Common risk factors in the development of Peutz-Jeghers syndrome are:
- STK11 (LKB1) gene mutation
- Family history of Peutz-Jeghers syndrome