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Australian Childhood Vision Impairment Register

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Description
This national Register collects information on children from birth to 18 years to establish the number of children with vision impairment, the causes and level of vision impairment, and other details such as additional disabilities. Data is used to provide better services and treatment for children. The Register is managed by the Royal Institute for Deaf and Blind Children, in partnership with service providers, corporate donors, government departments and health professionals.
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