Peutz-Jeghers syndrome classification: Difference between revisions

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Latest revision as of 16:40, 21 December 2017

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

There is no established classification system for Peutz-Jeghers syndrome.

There is no established classification system for Peutz-Jeghers syndrome.

@@ Line 1: / Line 1: @@
+__NOTOC__
 {{Peutz-Jeghers syndrome}}
+{{CMG}}; {{AE}} {{HQ}}
-{{CMG}}
 ==Overview==
+There is no established classification system for Peutz-Jeghers syndrome.
-'''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.
+==Classification==
+There is no established classification system for Peutz-Jeghers syndrome.
 == References ==
-<references />
+{{reflist|2}}
-{{Phakomatoses}}
+{{WH}}
-{{Digestive system neoplasia}}
+{{WS}}
-[[Category:Dental disorders]]
 [[Category:Gastroenterology]]
-[[Category:Genetic disorders]]
+[[Category:Surgery]]
 [[Category:Oncology]]
-[[Category:Syndromes]]
+[[Category:Disease]]
+[[Category:Pediatrics]]
+[[Category:Up-To-Date]]
-[[de:Peutz-Jeghers-Syndrom]]
-[[fr:Syndrome de Peutz-Jeghers]]
-[[it:Sindrome di Peutz-Jeghers]]
-[[nl:Syndroom van Peutz-Jeghers]]
-[[pl:Zespół Peutza-Jeghersa]]
-[[tr:Peutz-Jeghers sendromu]]
-{{WH}}
-{{WS}}