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

Osteogenesis imperfecta is a phenotypically and molecularly heterogeneous group of
inherited connective tissue disorders that share similar skeletal abnormalities causing bone …

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 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 …

Osteogenesis imperfecta is an inherited connective tissue disorder with wide phenotypic
and molecular heterogen-eity. A common issue associated with the molecular ab-normality …

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 (OI) is a rare disorder of type 1 collagen with 13 currently identified
types attributable to inherited abnormalities in type 1 collagen amount, structure, or …

Osteogenesis imperfecta is a systemic heritable disorder of connective tissue whose
cardinal manifestation is bone fragility. In approximately 90% of individuals with …

Osteogenesis Imperfecta (OI) is a group of connective tissue disorders with a broad range of
phenotypes characterized primarily by bone fragility. The prevalence of OI ranges from …

Osteogenesis imperfecta (OI), or brittle bone disease, is a heritable disorder characterized
by increased bone fragility. Four different types of the disease are commonly distinguished …