Osteogenesis imperfecta (OI) is a heritable bone dysplasia characterized by bone fragility
and long bone deformities. Approximately 85% of OI cases are caused by dominant …

Osteogenesis imperfecta (OI) is a crippling disorder whose primary manifestations are
fractures, bone deformity and bone pain. Children with OI have reduced mobility, require …

Osteogenesis imperfecta (OI) is the most common inherited form of bone fragility and
includes a heterogenous group of genetic disorders which most commonly result from …

Osteogenesis imperfecta (OI) is the most prevalent heritable bone fragility disorder in
children. It has been known for three decades that the majority of individuals with OI have …

Osteogenesis imperfecta (OI) is an inheritable disorder characterized by bone fragility with
various symptoms of connective tissue disorders. OI is commonly classified by Sillence's …

Osteogenesis Imperfecta (OI) is characterized by bone fragility. At least seven discrete types
have been described ranging from mild disease to a lethal form. In a large number of cases …

Osteogenesis imperfecta (OI) describes a group of rare heritable disorders of connective
tissue characterized by varying degrees of low bone mass and increased susceptibility to …

Osteogenesis imperfecta (OI) is in most cases a congenital disease of collagen type I with a
remarkable variation in phenotype, ranging from severe forms that result in perinatal death …

Osteogenesis imperfecta (OI) is a genetic bone fragility disorder characterized by low bone
mass, skeletal deformity, and variable short stature. OI is predominantly caused by dominant …

Osteogenesis imperfecta (OI) is a rare congenital disease with a wide spectrum of severity
characterized by skeletal deformity and increased bone fragility as well as additional …