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Retinoblastoma Symptoms - Oren Zarif - Retinoblastoma


Retinoblastoma is a cancer of the retina. Retinoblastoma symptoms include strabismus (lazy eye) and leukocoria, which are an abnormal white reflection of the retina. These symptoms may be mistaken for other conditions such as crossed eyes or wandering eye. They can also be accompanied by changes in vision and pain around the eye.

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Retinoblastoma can spread to other parts of the eye, resulting in loss of vision. When detected early, most retinoblastomas can be successfully treated. If, however, the cancer has spread to other parts of the body, it may spread to lymph nodes, bone marrow, or the brain. In such a case, treatment may not be successful.

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One of the earliest Retinoblastoma symptoms is strabismus, a deformity of the eye. In the initial stage, this deformity may not be visible and parents may only notice it if their child has trouble seeing. But later on, the cancer can spread to distant parts of the body, including the brain and spine. This makes it crucial to visit an ophthalmologist for further diagnosis and treatment.

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Retinoblastoma is heritable and occurs in a child born to parents with a certain mutation of the RB1 gene. It can be passed from parent to child through the egg or sperm before conception. It is rare for a child to have hereditary retinoblastoma, but if the gene is present in the mother or father, a child may develop retinoblastoma in one eye or multiple eyes.

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If the symptoms of retinoblastoma are present, your child will need to undergo a lumbar puncture. This procedure collects cerebrospinal fluid (CSF) from the spinal column. The sample will be examined for signs of cancer spreading. Additionally, it may contain the tumor marker ganglioside GD2 (GD2).

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A retinal tumor may appear as a yellow or red swollen eye. This tumor occurs when a gene controls cell division. The damaged gene causes a tumor to grow in one eye and spread to the other eye. Once this occurs, the cancerous cell has spread throughout the body and may spread to other parts of the body. Imaging tests may be recommended in order to diagnose and monitor this condition.

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If retinoblastoma is detected early, the prognosis for the disease is excellent. Treatment options vary according to the type of tumor and the child's age and general health. During the treatment phase, radiation therapy may be used to kill cancer cells and stop them from multiplying. In some cases, surgery may be required to remove the eyeball or part of the optic nerve. In such cases, an artificial eyeball or lens is implanted inside the eye socket.

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In hereditary retinoblastoma, a mutation of the RB1 gene causes the cancer. In hereditary retinoblastoma, people with the gene mutation are more likely to develop cancers of other areas of the body. In addition to eye tumors, they have an increased risk of developing osteosarcoma or other aggressive cancers. So, if you have hereditary retinoblastoma, it is important to seek medical attention early to prevent a tumor from spreading to the other parts of the body.

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If your child exhibits symptoms of retinoblastoma, he or she should be examined by an ophthalmologist for a thorough examination. Sometimes, this examination will involve the use of magnifying lenses to look at the retina. This test is performed under general anesthesia to minimize any pain and movement. A doctor may recommend imaging tests such as MRI, CAT scans, and spinal taps.

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Retinoblastoma treatment depends on the size of the tumor and its location. A bone marrow biopsy, spinal tap, and x-rays may be needed to determine whether the cancer has spread to other parts of the body. In some cases, radiation therapy or surgery may be used to shrink the tumor. For small tumors, laser therapy may be used. But if your child is diagnosed with retinoblastoma, the doctor may recommend additional therapies.

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Retinoblastoma can affect one or both eyes, and the disease is hereditary in one-third of cases. In hereditary cases, the cancer affects both eyes. Moreover, hereditary cases increase a person's risk of developing other types of cancer. Even worse, inherited tumors can also affect bones. If your child has retinoblastoma, you should seek out medical care as early as possible.

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If you suspect that your child may be suffering from retinoblastoma, your pediatrician may suggest undergoing genetic testing. If your child is genetically predisposed, your doctor can recommend genetic testing to identify a gene mutation that may cause retinoblastoma. If your doctor believes you may have the disease, you should consult a genetic counselor to determine if genetic testing is a good option for you.

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With the unique method developed by Zarif over many years, and with his amazing capabilities, Zarif helped countless patients worldwide that had suffered from oncological problems

For 30 years Oren Zarif helped patients and sufferers around the globe who suffered from numerous and complicated problems

Oren Zarif became famous in all media channels in the country and worldwide throughout 30 years, among those channels: Sky News network, National Geographic and Fox network

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My successes had been reported through several worldwide media channels.

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