Peutz-Jeghers syndrome other diagnostic studies: Difference between revisions
Jump to navigation
Jump to search
(Created page with "{{Peutz-Jeghers syndrome}} {{CMG}} ==Overview== '''Peutz-Jeghers''', also known as '''Hereditary Intestinal Polyposis Syndrome''', is an autosomal dominant [[genetic di...") |
m (Robot: Automated text replacement (-{{reflist}} +{{reflist|2}}, -<references /> +{{reflist|2}}, -{{WikiDoc Cardiology Network Infobox}} +)) |
||
Line 8: | Line 8: | ||
== References == | == References == | ||
{{reflist|2}} | |||
{{Phakomatoses}} | {{Phakomatoses}} |
Revision as of 13:49, 6 September 2012
Peutz-Jeghers syndrome Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Peutz-Jeghers syndrome other diagnostic studies On the Web |
American Roentgen Ray Society Images of Peutz-Jeghers syndrome other diagnostic studies |
Risk calculators and risk factors for Peutz-Jeghers syndrome other diagnostic studies |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
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.
References
Template:Digestive system neoplasia
de:Peutz-Jeghers-Syndrom
it:Sindrome di Peutz-Jeghers
nl:Syndroom van Peutz-Jeghers