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Rates of Down syndrome (DS) show considerable international variation, but a systematic assessment of this variation is lacking.
Government early intervention services for children with intellectual disability (ID) in Western Australia have adopted the model of family-centred care.
This study describes patterns of hospitalisations for children and young people with Down syndrome in Western Australia.
Data linkage is the bringing together of specific datasets from different sources using demographic information on individuals within a population.
Improved survival for children born with Down syndrome over the last 60 years has occurred incrementally, but disparities still exist
Mothers of a child with intellectual disability (ID) have more psychiatric disorders after the birth of their child than other mothers.
For mothers with intellectual disability, modifiable risk factors for adverse outcomes need addressing
There is an urgent need to develop high-quality falls prevention services for older adults with intellectual disability
Investigate impacts on maternal health and family quality of life in families with a child with the CDKL5 disorder
The aim of this study was to examine trends of Down syndrome (DS) in relation to maternal age and termination of pregnancies (ToP) in 20 registries