Background: Osteogenesis imperfecta (OI) is a disorder of bone formation leading to low mineral density and fractures. Children and adolescents with OI require periodic medical follow up, corrective surgery, drug therapy and physical therapy, as well as specific daily care practices. In addition, they have an increased incidence of fractures, which require immobilization and cause severe discomfort and short-term disability. This study evaluated the health-related quality of life of children and adolescents with OI in two reference centers for OI treatment in southern Brazil. Methods: In this prospective cross-sectional study, the Pediatric Quality of Life Inventory (PedsQLTM) was applied in two university-affiliated reference centers for O...
BACKGROUND: Osteogenesis Imperfecta (OI) is a rare genetic condition characterised by increased bone...
Osteogenesis imperfecta (OI) is a heterogeneous heritable connective tissue disorder characterized b...
Despite the growing interest in understanding the psycho-social impact of rare genetic diseases, few...
Abstract Background Osteogenesis imperfecta (OI) is a disorder of bone formation leading to low mine...
Background: Osteogenesis imperfecta (OI) is a disorder of bone formation leading to low mineral dens...
Background: Osteogenesis imperfecta (OI) is a group of genetic disorders of collagen biosynthesis, c...
Abstract Background Osteogenesis imperfecta (OI) affects dental and craniofacial development and may...
Osteogenesis imperfecta (OI) is a genetic disorder (prevalence: 1:10,000), leading to bone fragility...
Osteogenesis imperfecta, innate brittle bone disease, is a very serious disease. It is inheritable d...
Osteogenesis Imperfecta (OI) is a hereditary disorder effecting approximately 1 in 20,000 births. S...
Background Osteogenesis imperfecta (OI) is a group of rare inheritable disorders of connective tiss...
Background: Osteogenesis Imperfecta (OI) is a genetic condition resulting from a mutation in the gen...
To study (1). changes in anthropometrics, joint range of motion (ROM), muscle strength, functional a...
Caroline Marr,1,* Alison Seasman,1,* Nick Bishop2 1Metabolic Bone Disease Team, 2Academic Unit of Ch...
Osteogenesis imperfecta (OI) is a group of rare genetic disorders that affect bone formation. Patien...
BACKGROUND: Osteogenesis Imperfecta (OI) is a rare genetic condition characterised by increased bone...
Osteogenesis imperfecta (OI) is a heterogeneous heritable connective tissue disorder characterized b...
Despite the growing interest in understanding the psycho-social impact of rare genetic diseases, few...
Abstract Background Osteogenesis imperfecta (OI) is a disorder of bone formation leading to low mine...
Background: Osteogenesis imperfecta (OI) is a disorder of bone formation leading to low mineral dens...
Background: Osteogenesis imperfecta (OI) is a group of genetic disorders of collagen biosynthesis, c...
Abstract Background Osteogenesis imperfecta (OI) affects dental and craniofacial development and may...
Osteogenesis imperfecta (OI) is a genetic disorder (prevalence: 1:10,000), leading to bone fragility...
Osteogenesis imperfecta, innate brittle bone disease, is a very serious disease. It is inheritable d...
Osteogenesis Imperfecta (OI) is a hereditary disorder effecting approximately 1 in 20,000 births. S...
Background Osteogenesis imperfecta (OI) is a group of rare inheritable disorders of connective tiss...
Background: Osteogenesis Imperfecta (OI) is a genetic condition resulting from a mutation in the gen...
To study (1). changes in anthropometrics, joint range of motion (ROM), muscle strength, functional a...
Caroline Marr,1,* Alison Seasman,1,* Nick Bishop2 1Metabolic Bone Disease Team, 2Academic Unit of Ch...
Osteogenesis imperfecta (OI) is a group of rare genetic disorders that affect bone formation. Patien...
BACKGROUND: Osteogenesis Imperfecta (OI) is a rare genetic condition characterised by increased bone...
Osteogenesis imperfecta (OI) is a heterogeneous heritable connective tissue disorder characterized b...
Despite the growing interest in understanding the psycho-social impact of rare genetic diseases, few...