Osteogenesis imperfecta is a genetic disorder of increased bone fragility, low bone mass, and other connective-tissue manifestations. The most frequently used classification outlines four clinical types, which we have expanded to seven distinct types. In most patients the disorder is caused by mutations in one of the two genes encoding collagen type 1, but in some individuals no such mutations are detectable. The most important therapeutic advance is the introduction of bisphosphonate treatment for moderate to severe forms of osteogenesis imperfecta. However, at present, the best treatment regimen and the long-term outcomes of bisphosphonate therapy are unknown. Although this treatment does not constitute a cure, it is an adjunct to physiot...
Osteogenesis imperfecta (OI) is a heritable bone dysplasia characterized by bone fragility and long ...
Background: Osteogenesis imperfect is a disease of genetic origin, which causes a defect in the form...
Osteogenesis imperfecta is a heterogeneous group of inherited disorders chiefly affecting type I col...
Osteogenesis imperfecta is a heritable disorder of bone formation resulting in low bone mass and a p...
Osteogenesis imperfecta is a common heritable connective tissue disorder. Nearly ninety percent are ...
Osteogenesis imperfecta is a heritable condition characterized by abnormally brittle bones, with an ...
Osteogenesis imperfecta (OI), an inherited skeletal disorder characterized by low bone mass, bone fr...
Osteogenesis Imperfecta (OI) is a group of connective tissue disorders with a broad range of phenoty...
Osteogenesis imperfecta (OI) is a hereditary disease of the bones and fascia. It is associated with ...
Osteogenesis imperfecta (OI) is the most frequent hereditary bone disease during childhood. In most ...
The majority of patients with osteogenesis imperfecta (OI) have mutations in the COL1A1 or COL1A2 ge...
Osteogenesis imperfecta (OI) is a heterogeneous disease of connective tissue, the cardinal symptom b...
Osteogenesis imperfecta (OI) is a rare genetic disorder characterized by bone fragility and abnormal...
Osteogenesis imperfecta is one of the most commonly recognized inheritable disorders of the connecti...
Osteogenesis imperfecta is a rare genetic disorder that affects the production of collagen, causing ...
Osteogenesis imperfecta (OI) is a heritable bone dysplasia characterized by bone fragility and long ...
Background: Osteogenesis imperfect is a disease of genetic origin, which causes a defect in the form...
Osteogenesis imperfecta is a heterogeneous group of inherited disorders chiefly affecting type I col...
Osteogenesis imperfecta is a heritable disorder of bone formation resulting in low bone mass and a p...
Osteogenesis imperfecta is a common heritable connective tissue disorder. Nearly ninety percent are ...
Osteogenesis imperfecta is a heritable condition characterized by abnormally brittle bones, with an ...
Osteogenesis imperfecta (OI), an inherited skeletal disorder characterized by low bone mass, bone fr...
Osteogenesis Imperfecta (OI) is a group of connective tissue disorders with a broad range of phenoty...
Osteogenesis imperfecta (OI) is a hereditary disease of the bones and fascia. It is associated with ...
Osteogenesis imperfecta (OI) is the most frequent hereditary bone disease during childhood. In most ...
The majority of patients with osteogenesis imperfecta (OI) have mutations in the COL1A1 or COL1A2 ge...
Osteogenesis imperfecta (OI) is a heterogeneous disease of connective tissue, the cardinal symptom b...
Osteogenesis imperfecta (OI) is a rare genetic disorder characterized by bone fragility and abnormal...
Osteogenesis imperfecta is one of the most commonly recognized inheritable disorders of the connecti...
Osteogenesis imperfecta is a rare genetic disorder that affects the production of collagen, causing ...
Osteogenesis imperfecta (OI) is a heritable bone dysplasia characterized by bone fragility and long ...
Background: Osteogenesis imperfect is a disease of genetic origin, which causes a defect in the form...
Osteogenesis imperfecta is a heterogeneous group of inherited disorders chiefly affecting type I col...