"Shining Light on Retinoblastoma: Understanding and Conquering Childhood Eye Cancer"
Overview of Retinoblastoma
Retinoblastoma, a type of eye cancer primarily affecting children under 5 years old, is commonly detected before age 2 in about two-thirds of cases, with almost all cases diagnosed by age 5. Globally, an estimated 5000-8000 children develop retinoblastoma annually, with incidence rates varying by region.
Types and Symptoms
Retinoblastoma presents in two forms: bilateral (hereditary) and unilateral (non-hereditary). Symptoms often include leucocoria (abnormal white reflection in the eye) and squint (misaligned eye position).
Early Detection and Management
Early detection and diagnosis are crucial for effective treatment. A multidisciplinary approach involving Paediatric Ophthalmologists, Ophthalmic Oncologists, and Paediatric Oncologists is essential. Treatment aims to preserve life, vision, and the affected eye, with options such as radiotherapy, chemotherapy, and enucleation.
Importance of Vigilance
Parents, Pediatricians, and Ophthalmologists play a vital role in detecting signs of retinoblastoma during routine check-ups. Leucocoria, indicative of tumor presence, may be detected through comprehensive eye examination.
Connect with Drishti Eye Centre
For comprehensive eye care, including early detection and treatment of Retinoblastoma, trust Drishti Eye Centre for Vision & Eye Care.
Contact Us
🏢 Sri Nagar Colony Branch
📞 Call: 040-23742158, 8008133354
🏢 Gachibowli Branch
📞 Call: 040-49530998, 9966133354
🌐 For Online Appointment Visit: www.drishtieyecentre.org
