Considerable progress has been made in many aspects of osteogenesis imperfecta. The
international Sillence classification of osteogenesis imperfecta is being expanded to include …

Osteogenesis imperfecta is a genetic disorder that causes increased bone fragility and low
bone mass. Osteogenesis imperfecta is a rare disease: its estimated prevalence is between …

Osteogenesis imperfecta is a genetic disorder of increased bone fragility, low bone mass,
and other connective-tissue manifestations. The most frequently used classification outlines …

Abstract “Osteogenesis imperfecta” is a term used to describe a group of genetic disorders of
variable phenotype usually defined by recurrent fractures, low bone mass, and skeletal …

Osteogenesis imperfecta describes a group of heritable disorders characterized by
excessive bony fragility and reduced skeletal mass. It is classified in terms of its clinical …

Osteogenesis imperfecta is a heterogeneous group of genetic disorders that affect
connective tissue integrity, with bone fragility being the major clinical feature. Most forms of …

The last 2 years have seen additions proposed to the very limited armamentarium of
treatments for osteogenesis imperfecta. These include the use of bisphosphonates to …

Osteogenesis imperfecta is a rare hereditary disease mostly caused by mutations impairing
collagen synthesis and modification. Recently recessive forms have been described …

Osteogenesis imperfecta is a heritable disorder of bone formation resulting in low bone
mass and a propensity to fracture. It exhibits a broad range of clinical severity, ranging from …

Physiotherapy, rehabilitation, and orthopedic surgery are the mainstay of treatment in
moderate to severe forms of osteogenesis imperfecta (OI). Nevertheless, medical treatment …