Osteogenesis Imperfecta
Book AppointmentOsteogenesis imperfecta (OI) is a congenital bone disorder (meaning present at birth) causing fragile bones that can fracture easily. It is caused by a defect in the gene responsible for producing type 1 collagen, a protein used to build bones. OI can be mild to severe depending on the specific defect affecting the gene.
It is usually inherited. If you suffer from OI, there is a 50% chance that you will pass it on to your child. The disorder affects all races and genders equally.
A significant cause of this disorder are inter-marriages.
When to seek expert advise
Set a consultation with a doctor at the Department of Orthopaedics at The Aga Khan University Hospital if you notice the above mentioned symptoms in your child or if your child’s bones fracture with minimal force.
Disclaimer
The information provided on our website is for educational purposes and not intended to be a substitute for medical advice, diagnosis or treatment. You should always seek the advice of your doctor or other healthcare professional provider.
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