Renal oncocytoma risk factors: Difference between revisions
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==Overview== | ==Overview== | ||
Patients with tuberous sclerosis complex and Birt-Hogg-Dube syndrome are at an elevated risk of developing renal oncocytomas (often bilateral). | Patients with [[tuberous sclerosis complex]] and [[Birt-Hogg-Dubé syndrome|Birt-Hogg-Dube syndrome]] are at an elevated risk of developing renal oncocytomas (often bilateral). | ||
==Risk Factors== | ==Risk Factors== | ||
Patients with tuberous sclerosis complex and Birt-Hogg-Dube syndrome are at an elevated risk of developing renal oncocytomas (often bilateral). | Patients with [[tuberous sclerosis complex]] and [[Birt-Hogg-Dubé syndrome|Birt-Hogg-Dube syndrome]] are at an elevated risk of developing renal oncocytomas (often bilateral). | ||
==References== | ==References== | ||
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[[Category:Oncology]] | [[Category:Oncology]] | ||
[[Category:Nephrology]] | [[Category:Nephrology]] | ||
Latest revision as of 23:57, 29 July 2020
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Homa Najafi, M.D.[2] Shanshan Cen, M.D. [3]
Overview
Patients with tuberous sclerosis complex and Birt-Hogg-Dube syndrome are at an elevated risk of developing renal oncocytomas (often bilateral).
Risk Factors
Patients with tuberous sclerosis complex and Birt-Hogg-Dube syndrome are at an elevated risk of developing renal oncocytomas (often bilateral).