Caroline Marr,1,* Alison Seasman,1,* Nick Bishop2 1Metabolic Bone Disease Team, 2Academic Unit of Child Health, Department of Human Metabolism, University of Sheffield, Sheffield Children’s NHS Foundation Trust, Sheffield, UK *These authors contributed equally to this work Abstract: Osteogenesis imperfecta (OI) is a heterogeneous heritable connective tissue disorder characterized by low bone density. The type and severity of OI are variable. The primary manifestations are fractures, bone deformity, and bone pain, resulting in reduced mobility and function to complete everyday tasks. OI affects not only the physical but also the social and emotional well-being of children, young people, and their families. As such, medical, surgical, a...
Osteogenesis Imperfecta (OI) is a group of connective tissue disorders with a broad range of phenoty...
Osteogenesis imperfecta (OI) is a genetic disorder that is usually caused by disturbed production of...
Osteogenesis imperfecta (OI) is the most common bone genetic disorder and it ischaracterized by bone...
Osteogenesis imperfecta (OI) is a heterogeneous heritable connective tissue disorder characterized b...
Osteogenesis imperfecta (OI) is a heritable bone dysplasia characterized by bone fragility and long ...
Osteogenesis imperfecta (OI) is the most frequent hereditary bone disease during childhood. In most ...
Osteogenesis imperfecta (OI) is a genetic disorder (prevalence: 1:10,000), leading to bone fragility...
Osteogenesis imperfecta (OI), an inherited skeletal disorder characterized by low bone mass, bone fr...
Despite the growing interest in understanding the psycho-social impact of rare genetic diseases, few...
Osteogenesis imperfecta is an inherited connective tissue disorder with wide phenotypic and molecula...
Background: Osteogenesis imperfecta (OI) is a disorder of bone formation leading to low mineral dens...
BACKGROUND: Osteogenesis Imperfecta (OI) is a rare genetic condition characterised by increased bone...
Osteogenesis imperfecta is an inherited connective tissue disorder with wide phenotypic and molecula...
BACKGROUND This report describes a new strategy for the care of patients with osteogenesi...
Osteogenesis imperfecta, innate brittle bone disease, is a very serious disease. It is inheritable d...
Osteogenesis Imperfecta (OI) is a group of connective tissue disorders with a broad range of phenoty...
Osteogenesis imperfecta (OI) is a genetic disorder that is usually caused by disturbed production of...
Osteogenesis imperfecta (OI) is the most common bone genetic disorder and it ischaracterized by bone...
Osteogenesis imperfecta (OI) is a heterogeneous heritable connective tissue disorder characterized b...
Osteogenesis imperfecta (OI) is a heritable bone dysplasia characterized by bone fragility and long ...
Osteogenesis imperfecta (OI) is the most frequent hereditary bone disease during childhood. In most ...
Osteogenesis imperfecta (OI) is a genetic disorder (prevalence: 1:10,000), leading to bone fragility...
Osteogenesis imperfecta (OI), an inherited skeletal disorder characterized by low bone mass, bone fr...
Despite the growing interest in understanding the psycho-social impact of rare genetic diseases, few...
Osteogenesis imperfecta is an inherited connective tissue disorder with wide phenotypic and molecula...
Background: Osteogenesis imperfecta (OI) is a disorder of bone formation leading to low mineral dens...
BACKGROUND: Osteogenesis Imperfecta (OI) is a rare genetic condition characterised by increased bone...
Osteogenesis imperfecta is an inherited connective tissue disorder with wide phenotypic and molecula...
BACKGROUND This report describes a new strategy for the care of patients with osteogenesi...
Osteogenesis imperfecta, innate brittle bone disease, is a very serious disease. It is inheritable d...
Osteogenesis Imperfecta (OI) is a group of connective tissue disorders with a broad range of phenoty...
Osteogenesis imperfecta (OI) is a genetic disorder that is usually caused by disturbed production of...
Osteogenesis imperfecta (OI) is the most common bone genetic disorder and it ischaracterized by bone...