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Difference between revisions of "Familial adenomatous polyposis"
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Familial adenomatous polyposis (view source)
Revision as of 17:32, 3 September 2011
, 17:32, 3 September 2011+Turcot syn.
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#*Less polyps - typically 10 to 100.<ref name=pmid19822006>{{cite journal |author=Half E, Bercovich D, Rozen P |title=Familial adenomatous polyposis |journal=Orphanet J Rare Dis |volume=4 |issue= |pages=22 |year=2009 |pmid=19822006 |pmc=2772987 |doi=10.1186/1750-1172-4-22 |url=}}</ref> | #*Less polyps - typically 10 to 100.<ref name=pmid19822006>{{cite journal |author=Half E, Bercovich D, Rozen P |title=Familial adenomatous polyposis |journal=Orphanet J Rare Dis |volume=4 |issue= |pages=22 |year=2009 |pmid=19822006 |pmc=2772987 |doi=10.1186/1750-1172-4-22 |url=}}</ref> | ||
#**As one my think... they tend to get cancer later than (the plain vanilla) FAP. | #**As one my think... they tend to get cancer later than (the plain vanilla) FAP. | ||
===Gardner syndrome=== | |||
===Turcot syndrome=== | |||
FAP associated with a [[medulloblastoma]].<ref name=pmid19822006>{{Cite journal | last1 = Half | first1 = E. | last2 = Bercovich | first2 = D. | last3 = Rozen | first3 = P. | title = Familial adenomatous polyposis. | journal = Orphanet J Rare Dis | volume = 4 | issue = | pages = 22 | month = | year = 2009 | doi = 10.1186/1750-1172-4-22 | PMID = 19822006 | PMC = 2772987}}</ref> | |||
==Associations== | ==Associations== | ||