Retinoblastoma risk factors: Difference between revisions
Simrat Sarai (talk | contribs) No edit summary |
Simrat Sarai (talk | contribs) No edit summary |
||
| Line 6: | Line 6: | ||
==Common Risk Factors== | ==Common Risk Factors== | ||
==Family History== | |||
Approximately 10% of patients with retinoblastoma have a previously established family history of the disease. | Approximately 10% of patients with retinoblastoma have a previously established family history of the disease. | ||
Revision as of 04:25, 11 October 2015
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Simrat Sarai, M.D. [2]
|
Retinoblastoma Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
Retinoblastoma risk factors On the Web |
|
American Roentgen Ray Society Images of Retinoblastoma risk factors |
|
Risk calculators and risk factors for Retinoblastoma risk factors |
Overview
Common risk factors in the development of retinoblastoma are, advanced paternal age, positive family history, and viral exposure.
Common Risk Factors
Family History
Approximately 10% of patients with retinoblastoma have a previously established family history of the disease.
Viral exposure
The presence of HPV sequences in retinoblastoma tumor tissue may play a role in the development of sporadic retinoblastoma.
Advanced paternal age
There is evidence suggesting that the mutations of RB1 are more common during spermatogenesis than oogenesis.