Reach Us +1 218 451 2974
Retinoblastoma: Identifying the Diagnostic Signs for Early Treatment | OMICS International | Abstract
ISSN: 2376-0281

International Journal of Neurorehabilitation
Open Access

Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)

Review Article

Retinoblastoma: Identifying the Diagnostic Signs for Early Treatment

Simon B N Thompson1,2*, Holly Chinnery1, Siamak Noroozi3, Bryce Dyer3 and Ken Barratt4

1Psychology Research Centre, Faculty of Science & Technology, Bournemouth University, UK

2International Scientific Council for Research, Université Paris X Ouest Nanterre La Défense, France

3Design Simulation Research Centre, Faculty of Science & Technology, Bournemouth University, UK

4National Artificial Eye Service, National Health Service, Blackpool, UK

Corresponding Author:
Simon B N Thompson
Associate Professor of Clinical Psychology & Neuropsychology Psychology Research Centre,
Faculty of Science & Technology Bournemouth University, Poole, BH12 5BB, UK
01202 961558
[email protected]

Received Date: February 27, 2015; Accepted Date: April 22 2015; Published Date: April 28 2015

Citation: Thompson SBN,Chinnery H, Noroozi S, Dyer B, Barratt K (2015) Retinoblastoma: Identifying the Diagnostic Signs for Early Treatment. Int J Neurorehabilitation 2:160. doi:10.4172/2376-0281.1000160

Copyright: © 2015 Thompson SBN, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.


Retinoblastoma is a rare but significant cause of childhood eye cancer world-wide. The prognosis depends upon early diagnosis and treatment but also upon accurate classification of the tumours. Unilateral incidence is normally non-hereditary compared with bilateral incidence where secondary tumours are more common. Survivorship is much better for unilateral compared with bilateral and trilateral retinoblastoma. Early signs are important to detect and photography can assist in identifying no return of “red-eye” during flash photography and yellow appearance of the tumour. Treatment options are discussed together with new psycho-oncology approaches that address potential trauma in the survivor as well as in the family of the survivor.


Recommended Conferences

Global Experts Meet on Neurology and Neuropsychiatry

Amsterdam, Netherlands

4th European Congress on Nephrology & Renal Care

Capetown, South Africa
Share This Page