Osteogenesis imperfecta (OI) is a metabolic bone disorder commonly encountered in orthopaedic practice within the context of a multidisciplinary team. Although relatively rare, it is among the most researched of the skeletal dysplasias, making it challenging for the general orthopaedic surgeon to keep abreast with current evidence. The aim of this review article is to provide a comprehensive overview of OI for the general orthopaedic surgeon. It touches on the relevant epidemiology, pathology and clinical aspects of the condition. A discussion of the background and current topical issues surrounding the classification systems, and the medical and orthopaedic management aspects follows. The main focus of this review is on the peri-operative ...
Osteogenesis imperfecta (OI) is a heritable bone dysplasia characterized by bone fragility and long ...
Osteogenesis imperfecta (OI) is the most common genetic bone disorder. The exact incidence of OI is ...
The authors present a case of Osteogenesis Imperfecta, emphasizing the clinical and epidemiological ...
Osteogenesis imperfecta (OI) is a metabolic bone disorder commonly encountered in orthopaedic practi...
Osteogenesis imperfecta (OI), an inherited skeletal disorder characterized by low bone mass, bone fr...
Osteogenesis imperfecta (OI) is a hereditary disease of the bones and fascia. It is associated with ...
Osteogenesis Imperfecta (OI) is a group of connective tissue disorders with a broad range of phenoty...
Introduction Osteogenesis imperfecta (OI) is a group of rare and relatively diverse genetic disorder...
Osteogenesis imperfecta (OI) is a heterogeneous heritable connective tissue disorder characterized b...
Osteogenesis imperfecta (OI) is a genetic disorder that is usually caused by disturbed production of...
Osteogenesis imperfecta or brittle bone disease, a heritable disorder of connective tissue, is the m...
Osteogenesis imperfecta (OI) is a connective tissue disorder that is caused by genetic mutation. OI ...
The constantly changing information about the genetic nature of osteogenesis imperfecta (OI), new ap...
Osteogenesis imperfecta (OI) is the most frequent hereditary bone disease during childhood. In most ...
Fractures in patients with osteogenesis imperfecta (OI) are caused by a decreased strength of bone d...
Osteogenesis imperfecta (OI) is a heritable bone dysplasia characterized by bone fragility and long ...
Osteogenesis imperfecta (OI) is the most common genetic bone disorder. The exact incidence of OI is ...
The authors present a case of Osteogenesis Imperfecta, emphasizing the clinical and epidemiological ...
Osteogenesis imperfecta (OI) is a metabolic bone disorder commonly encountered in orthopaedic practi...
Osteogenesis imperfecta (OI), an inherited skeletal disorder characterized by low bone mass, bone fr...
Osteogenesis imperfecta (OI) is a hereditary disease of the bones and fascia. It is associated with ...
Osteogenesis Imperfecta (OI) is a group of connective tissue disorders with a broad range of phenoty...
Introduction Osteogenesis imperfecta (OI) is a group of rare and relatively diverse genetic disorder...
Osteogenesis imperfecta (OI) is a heterogeneous heritable connective tissue disorder characterized b...
Osteogenesis imperfecta (OI) is a genetic disorder that is usually caused by disturbed production of...
Osteogenesis imperfecta or brittle bone disease, a heritable disorder of connective tissue, is the m...
Osteogenesis imperfecta (OI) is a connective tissue disorder that is caused by genetic mutation. OI ...
The constantly changing information about the genetic nature of osteogenesis imperfecta (OI), new ap...
Osteogenesis imperfecta (OI) is the most frequent hereditary bone disease during childhood. In most ...
Fractures in patients with osteogenesis imperfecta (OI) are caused by a decreased strength of bone d...
Osteogenesis imperfecta (OI) is a heritable bone dysplasia characterized by bone fragility and long ...
Osteogenesis imperfecta (OI) is the most common genetic bone disorder. The exact incidence of OI is ...
The authors present a case of Osteogenesis Imperfecta, emphasizing the clinical and epidemiological ...