Osteogenesis imperfecta
What is Osteogenesis imperfecta?
A rare, genetic, primary bone dysplasias characterized by increased bone fragility, low bone mass, and susceptibility to bone fractures. The clinical severity is heterogeneous.
Other condition names
- Brittle bone disease
- Glass bone disease
- Lobstein disease
- OI
- Osteopsathyrosis
- Porak and Durante disease
Inheritance type
Autosomal dominant, Autosomal recessive, X-linked recessive
Prevalence
- Worldwide: 1-5 in 10,000
Age of Onset
- All ages
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on "https://www.orphadata.com". Data version 1.3.16 / 4.1.7.