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==Case Report==
*Young patient with hyperpigmentation of oral mucosa.<ref name="DuanWang2017">{{cite journal|last1=Duan|first1=Shou-Xing|last2=Wang|first2=Guang-Huan|last3=Zhong|first3=Jun|last4=Ou|first4=Wen-Hui|last5=Fu|first5=Ma-Xian|last6=Wang|first6=Fu-Sheng|last7=Ma|first7=Shu-Hua|last8=Li|first8=Jian-Hong|title=Peutz–Jeghers syndrome with intermittent upper intestinal obstruction|journal=Medicine|volume=96|issue=17|year=2017|pages=e6538|issn=0025-7974|doi=10.1097/MD.0000000000006538}}</ref>


*Family and patient tested for Peutz-Jeghers syndrome STK11 mutation.
**10 out of 14 family members were diagnosed with Peutz-Jeghers syndrome.
*Patient was discovered to have polys in the stomach.
*Patient recovered well.
== References ==
== References ==
{{reflist|2}}
{{reflist|2}}

Latest revision as of 18:06, 19 December 2017

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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]

Case Report

  • Young patient with hyperpigmentation of oral mucosa.[1]
  • Family and patient tested for Peutz-Jeghers syndrome STK11 mutation.
    • 10 out of 14 family members were diagnosed with Peutz-Jeghers syndrome.
  • Patient was discovered to have polys in the stomach.
  • Patient recovered well.

References

  1. Duan, Shou-Xing; Wang, Guang-Huan; Zhong, Jun; Ou, Wen-Hui; Fu, Ma-Xian; Wang, Fu-Sheng; Ma, Shu-Hua; Li, Jian-Hong (2017). "Peutz–Jeghers syndrome with intermittent upper intestinal obstruction". Medicine. 96 (17): e6538. doi:10.1097/MD.0000000000006538. ISSN 0025-7974.