Peutz-Jeghers syndrome other diagnostic studies: Difference between revisions

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==Overview==
==Overview==
Other diagnostic studies for Peutz-Jeghers syndrome include [[colonoscopy]] and [[capsule endoscopy]], which demonstrate multiple [[polyps]] in the [[colon]] and in the [[small intestine]], respectively.
==Other Diagnostic Studies==
Other diagnostic studies for Peutz-Jeghers syndrome include:<ref name="Tomas2014">{{cite journal|last1=Tomas|first1=Catherine|title=Update on imaging of Peutz-Jeghers syndrome|journal=World Journal of Gastroenterology|volume=20|issue=31|year=2014|pages=10864|issn=1007-9327|doi=10.3748/wjg.v20.i31.10864}}</ref>


'''Peutz-Jeghers''', also known as '''Hereditary Intestinal Polyposis Syndrome''', is an [[autosomal dominant]] [[genetic disease]] characterized by the development of benign hamartomatous polyps in the gastrointestinal tract.
*[[Genetic testing]] (Gold standard):
:*[[Genetic testing]] for ''[[STK11]]'' (''LKB1'')  [[gene]]
*[[Colonoscopy]]
*[[Capsule endoscopy]]


== References ==
== References ==
<references />
{{reflist|2}}


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Latest revision as of 16:51, 21 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

Other diagnostic studies for Peutz-Jeghers syndrome include colonoscopy and capsule endoscopy, which demonstrate multiple polyps in the colon and in the small intestine, respectively.

Other Diagnostic Studies

Other diagnostic studies for Peutz-Jeghers syndrome include:[1]

References

  1. Tomas, Catherine (2014). "Update on imaging of Peutz-Jeghers syndrome". World Journal of Gastroenterology. 20 (31): 10864. doi:10.3748/wjg.v20.i31.10864. ISSN 1007-9327.

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