In this Article
- What causes retinoblastoma?
- Who gets retinoblastoma?
- What are the symptoms of retinoblastoma?
- How is retinoblastoma diagnosed?
- What Are the Stages of Retinoblastoma?
- How Is Retinoblastoma Treated?
- What Does the Future Hold for People With Retinoblastoma?
- Is Retinoblastoma Preventable?
- Find a local Eye Doctor in your town
What Does the Future Hold for People With Retinoblastoma?
Over 90% of children will survive more than five years after being diagnosed with retinoblastoma. Patients are able to retain about 85% of vision in the affected eye after treatment.
Hereditary forms of retinoblastoma are more likely to reoccur years after treatment; therefore, close follow-up after treatment is important for these patients.
Is Retinoblastoma Preventable?
Because heredity and age play such large roles in retinoblastoma, the best prevention is through early detection. All babies should have a general eye exam at birth and then again at six months. A doctor will be able to detect any serious congenital problems or the appearance of retinal tumors. Newborns with a family history of retinoblastoma should have a thorough eye exam a few days after birth, at six weeks, once every three months until age two, and once every four months until age three. The chance is 1 in 2 that a parent will pass on the DNA mutation that causes retinoblastoma. A blood test can be used to determine if this mutation is present.
For adults, prevention means getting a thorough regular eye examination at least once a year and more often, as recommended by your ophthalmologist, if you have a personal or family history of eye disorders or diabetes.
Reviewed by the doctors at The Cleveland Clinic Cole Eye Institute.
Edited by Charlotte E. Grayson, MD, WebMD, November 2004.
Portions of this page copyright © The Cleveland Clinic 2000-2004
Last Editorial Review: 1/31/2005 5:59:00 AM
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