Retinoblastoma: concerning its initiation and treatment.

Abstract:

:Retinoblastoma (RB) is the most common intraocular cancer of infancy and childhood. This cancer is initiated by mutation on RB1, the tumor suppressor gene that is responsible for the regulation of both cell cycle and gnome stability in retinal cells. Patients with a constitutional mutation on RB1 can be inherited. RB occurs approximately 1 in every 15 000-20 000 live births. The worldwide mortality for this cancer is about 5%-11%. However, this rate rises to about 40%-70% in developing countries due to a delay in diagnosis. A wide variety of options are available for the treatment, but often a combination of therapies is adopted to optimize individualized care.

journal_name

Int J Ophthalmol

authors

Luo C,Deng YP

doi

10.3980/j.issn.2222-3959.2013.03.26

subject

Has Abstract

pub_date

2013-06-18 00:00:00

pages

397-401

issue

3

eissn

2222-3959

issn

2227-4898

pii

ijo-06-03-397

journal_volume

6

pub_type

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