Retinoblastoma

Retinoblastoma is a rare inherited Cancer of the retina, which occurs in infancy. It may affect one or both eyes, and usually present before the age of three either with visual loss, squint or the replacement of the normal red reflex in the pupil with a white reflex. Since these are usually hereditary, and can be cured (and vision preserved) if treated early, the children of affected parents should be screened regularly.
 
 

This information is licensed for use by Wellbeing Information Systems Ltd ("WIS"), and protected by international copyright law. All rights are reserved. (email info@wisinfo.co.uk).
The information provided by WIS is for guidance only. Whilst it is based upon the expert advice of leading professionals, and extensive research, it is not a substitute for diagnosis by a qualified professional. Always consult your doctor, pharmacist or qualified practitioner before making any changes or additions to prescribed medication.