Retinoblastoma
ORPHA:790· ICD-10 C69.2
Definition
A rare eye tumor disease representing the most common intraocular malignancy in children. It is a life threatening neoplasia but is potentially curable and it can be hereditary or non hereditary, unilateral or bilateral.
- Prevalence
- 1-9 / 100 000
- Inheritance
- Autosomal dominant, Not applicable
- Age of onset
- Antenatal, Childhood, Infancy