Bruck syndrome
ORPHA:2771· ICD-10 M21.8
Definition
A rare genetic bone disease characterized by the association of osteogenesis imperfecta and congenital joint contractures.
- Prevalence
- <1 / 1 000 000
- Inheritance
- Autosomal recessive
- Age of onset
- Antenatal, Childhood, Infancy, Neonatal