Trabecular Architecture During Growth - Does It Determine Metaphyseal Peak Bone Strength In Adulthood?
Funder
National Health and Medical Research Council
Funding Amount
$165,339.00
Summary
Skeletal fragility is common is elderly people but has its origin in childhood. Strong bone established during growth will provide more protection against occurrence of fragility fracture in old age. Identifying individuals during childhood who are at high risk of skeletal fragility, and early intervention is a strategic approach managing the burden of skeletal fragility on the ageing population.
A Longitudinal Study Of Bone Development In Children
Funder
National Health and Medical Research Council
Funding Amount
$144,750.00
Summary
Osteoporosis is a major public health problem resulting in 50-75,000 fractures each year in Australia costing the community about 800 million dollars per annum. Bone strength is a risk factor for fractures in both childhood and in later life. Relatively little is known about bone development with the exception of calcium intake and physical activity. This study will follow 500 children from birth in 1988 to 2004 with the aim of understanding the contribution of lifestyle factors to bone developm ....Osteoporosis is a major public health problem resulting in 50-75,000 fractures each year in Australia costing the community about 800 million dollars per annum. Bone strength is a risk factor for fractures in both childhood and in later life. Relatively little is known about bone development with the exception of calcium intake and physical activity. This study will follow 500 children from birth in 1988 to 2004 with the aim of understanding the contribution of lifestyle factors to bone development in this time period.Read moreRead less
A Subphenotyping Approach To Identifying Genes Responsible For Isolated Clefts Of The Lip And Palate.
Funder
National Health and Medical Research Council
Funding Amount
$679,707.00
Summary
Clefts of the lip and palate are the most common birth defects involving the face. The genes responsible for these conditions have been difficult to find in the past. We have identified a method through which the chances of finding these genes is greatly increased. Detailed measurements of a number of facial features in cleft patients and unaffected first-degree relatives will provide a much clearer picture of those at higher risk of being affected by this debilitating disorder.