Retinoblastoma is a rare eye cancer that typically affects young children. Early intervention is crucial to save the child's life and preserve vision.
Retinoblastoma is a rare, malignant tumor of the retina, the light-sensitive tissue at the back of the eye. It usually occurs in young children. Timely detection and a targeted treatment approach are critical to maximizing the chances of curing the cancer and preserving as much vision as possible.
To achieve complete remission, prevent relapse, and ensure long-term survival with the best possible quality of life.
