Hamartoma risk factors: Difference between revisions
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==Overview== | ==Overview== | ||
The most potent risk factor in the development of hamartomas is familial | The most potent risk factor in the development of hamartomas is familial inheritance.<ref name="pmid26739631">{{cite journal |vauthors=Richardson MS |title=Familiar and unfamiliar pseudoneoplastic lesions of the head and neck |journal=Semin Diagn Pathol |volume=33 |issue=1 |pages=24–30 |year=2016 |pmid=26739631 |doi=10.1053/j.semdp.2015.09.004 |url=}}</ref> | ||
==Risk factors== | ==Risk factors== | ||
The most potent risk factor in the development of hamartomas is familial inheritance.<ref name="pmid26739631">{{cite journal |vauthors=Richardson MS |title=Familiar and unfamiliar pseudoneoplastic lesions of the head and neck |journal=Semin Diagn Pathol |volume=33 |issue=1 |pages=24–30 |year=2016 |pmid=26739631 |doi=10.1053/j.semdp.2015.09.004 |url=}}</ref> | |||
==References== | ==References== | ||
{{reflist| | {{reflist|1}} | ||
[[Category:Disease]] | [[Category:Disease]] |
Revision as of 18:01, 26 January 2016
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Maria Fernanda Villarreal, M.D. [2]
Overview
The most potent risk factor in the development of hamartomas is familial inheritance.[1]
Risk factors
The most potent risk factor in the development of hamartomas is familial inheritance.[1]
References