Retinoblastoma is an eye cancer that begins in the retina — the sensitive lining on the inside of your eye. Retinoblastoma most commonly affects young children, but can rarely occur in adults.<\/p>\n
Your retina is made up of nerve tissue that senses light as it comes through the front of your eye. The retina sends signals through your optic nerve to your brain, where these signals are interpreted as images. <\/p>\n
A rare form of eye cancer, retinoblastoma is the most common form of cancer affecting the eye in children. Retinoblastoma may occur in one or both eyes.<\/p>\n
Retinoblastoma occurs when nerve cells in the retina develop genetic mutations. These mutations cause the cells to continue growing and multiplying when healthy cells would die. This accumulating mass of cells forms a tumor. Retinoblastoma cells can invade further into the eye and nearby structures. Retinoblastoma can also spread (metastasize) to other areas of the body, including the brain and spine. <\/p>\n
In the majority of cases, it’s not clear what causes the genetic mutations that lead to retinoblastoma. However, it’s possible for children to inherit a genetic mutation from their parents. <\/p>\n
Retinoblastoma that is inherited<\/strong> <\/p>\n Gene mutations that increase the risk of retinoblastoma and other cancers can be passed from parents to children. Hereditary retinoblastoma is passed from parents to children in an autosomal dominant pattern, which means only one parent needs a single copy of the mutated gene to pass the increased risk of retinoblastoma on to the children. If one parent carries a mutated gene, each child has a 50 percent chance of inheriting that gene. <\/p>\n Although a genetic mutation increases a child’s risk of retinoblastoma, it doesn’t mean that cancer is inevitable. <\/p>\n Children with the inherited form of retinoblastoma tend to develop the disease at an earlier age. Hereditary retinoblastoma also tends to occur in both eyes, as opposed to just one eye.<\/p>\n Signs of retinoblastoma include: <\/p>\n
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Make an appointment with your child’s doctor if you notice any changes to your child’s eyes that concern you. Retinoblastoma is a rare cancer, so your child’s doctor may explore other more common eye conditions first. <\/p>\n If you have a family history of retinoblastoma, ask your pediatrician when your child should begin regular eye exams to screen for retinoblastoma.<\/p>\n","protected":false},"excerpt":{"rendered":"SYMPTOMS<\/h2>\n
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When to see a doctor<\/strong> <\/p>\n