Retinoblastoma Symptoms - Oren Zarif - Retinoblastoma

The most common Retinoblastoma symptom is a white pupil. The white pupil is an opening in the center of the eye that is often enlarged and cloudy in color. Parents usually notice it when taking photos of their children using a flash. If your child's vision becomes worse, it's important to see a pediatric eye doctor. This disease has no cure yet.

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A physical exam is conducted to check general health and any abnormalities. Doctors also ask about a child's family history to determine the likelihood of retinoblastoma. The child will undergo a dilated pupil exam, which involves opening the pupil with eye drops and examining the retina and optic nerve. In very young children, the exam may require anesthetic.

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The mutation that causes retinal tumors usually occurs later in embryonic development. It affects the eye's cells and cannot be passed on to offspring. It rarely spreads beyond the eye, though it can spread to the brain and bones along the optic nerve. A large retinoblastoma can affect vision and may produce very few other symptoms. A few other symptoms may occur, such as a loss of appetite and vomiting.

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If you suspect a child has Retinoblastoma, your child should visit a pediatric eye specialist. This is because this disease can mimic other conditions. For example, a child may be losing weight or having trouble focusing. You should visit a pediatric eye doctor if you notice these symptoms. It's essential to rule out other causes before a treatment can be initiated.

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When a child has Retinoblastoma, the pupil is cloudy white. The tumor is usually hereditary, and about one in three children has a mutation in the RB1 gene. The gene is found in all cells of the body, so any mutation in one eye may result in the development of the disease in the other. And the disease usually occurs at the eye before the child is a year old.

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The most common Retinoblastoma symptom is the white pupil. This can look like a cat's eye reflex. This is different from the red-eye effect in flash photos. It's common for parents to notice the symptom first. But if you suspect a child has Retinoblastoma, it's vital to seek medical attention right away.

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After a diagnosis of Retinoblastoma, your child will have periodic checkups. These may include eye examinations under anesthesia and follow-ups with an oncologist. Your child may need a prosthesis or a glass eye. Treatment for Retinoblastoma is usually very successful as long as it is detected early enough. If detected in its early stages, it may cure the child's disease.

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Hereditary Retinoblastoma is caused by a genetic mutation in genes that control eye development. This condition is inherited from one parent or may develop spontaneously during embryonic development. Inheritance is one of the main risk factors for developing Retinoblastoma, with about 25 to 30 percent of affected children passing it on to their children. If one parent is affected, the mutation is passed on to the offspring, and most will develop the disease. Retinoblastoma is hereditary in almost all children with cancer of the eye, and in around 15 percent of patients with the disease in one eye.

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If you experience any of these Retinoblastoma symptom, it's important to see a doctor as soon as possible. Treatment for this disease is crucial in ensuring that you're not suffering from this rare disease. The disease rarely spreads to other parts of the body. The sooner you seek medical attention, the better. You can be treated, and in most cases, you'll be cured of Retinoblastoma.