retinoblastoma in A Sentence

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Retinoblastoma usually occurs in children around the age of 2 years.

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Retinoblastoma is the most common type of eye cancer in children worldwide.

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Intraocular: In intraocular Retinoblastoma, the cancer has not spread beyond the eye.

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These children will therefore have a high risk of developing Retinoblastoma themselves.

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When Retinoblastoma is diagnosed, it is classified into one of three major stages.

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The management of Retinoblastoma has improved tremendously and it is now a largely curable disease.

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Retinoblastoma is a common type of childhood cancer and a leading cause of blindness in children.

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Children with heritable Retinoblastoma will be given genetic counselling when they are old enough to understand.

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Children with heritable Retinoblastoma will be given genetic counselling when they are old enough to understand it.

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The size of the Retinoblastoma tumor could also be a limiting factor in the favorable outcome of the injection.

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However, they include melanoma(which typically affects the choroid layer and is usually a tumour of later life) and Retinoblastoma.

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Also, people who have been treated with soft tissue sarcoma and Retinoblastoma also raise the risk of suffering of bone cancer.

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Where there is no family history, the first sign of Retinoblastoma is often a white pupil that does not reflect the light.

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Until now, scientists have lamented that the only cure for the childhood eye cancer Retinoblastoma is surgical removal of the affected eye.

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If radiation therapy is used to treat Retinoblastoma, the risk of osteosarcoma in the bones around the eye is even higher.

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Now, in a recent report published in Science Translational Medicine, scientists have found another approach to target Retinoblastoma using safer: cancer-killing viruses.

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If radiation therapy is used to treat the Retinoblastoma, the risk of osteosarcoma in the bones around the eye is even higher.

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If there's no family history of Retinoblastoma, the first sign of the condition is often a white pupil that does not reflect light(leucocoria).

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Call your provider if signs or symptoms of Retinoblastoma are present, especially if your child's eyes look abnormal or appear abnormal in photographs.

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Also, if radiation therapy is used to treat the Retinoblastoma, the risk of osteosarcoma in the bones around the eye is even higher.

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When diagnosed in its early stage, Retinoblastoma has not spread outside the eye and is very treatable- even curable- in 95 percent of cases.

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Call your health care provider if signs or symptoms of Retinoblastoma are present, especially if your child's eyes look abnormal or appear abnormal in photographs.

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Retinoblastoma can be inherited, but this only accounts for about 45 percent of cases, meaning the majority of cases are not connected to a family history.

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Based on computational modelling, researchers at the Indian Institute of Technology(IIT) Madras have identified the biochemical pathways that eye cancer(Retinoblastoma) preferentially chooses for growth and survival.

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Retinoblastoma can sometimes be an inherited condition, so any family history of the disease- or other forms of cancer- is very important to discuss with a healthcare professional.

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This operation is generally recommended in dire circumstances- such as in advanced cases of Retinoblastoma, for example- and when there are no other options, or if an eye is blind and painful.

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Here's Reulen's recommendation: If you received high-dose radiation or had childhood cancers with a genetic component(such a Retinoblastoma, a cancer that affects the eye), work with your doctor to keep a closer watch for new cancers.

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She thanked me for the donation, and she explained that she is studying Retinoblastoma, which is a deadly cancer of the retina that affects children under the age of five, and she said that yes, we were invited to visit her lab.

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