The aim of our study was to compare the surgical and conservative treatment of patients affected by fragility fractures and deformities of long bones in osteogenesis imperfecta (OI). Our series consisted of 29 consecutive OI patients treated at our Institute. The series comprised 14 females and 15 males of different ages. The mean age at the time of the first treatment was 8 years (median 6 years; SD ± 15; range 1 to 75). The mean follow-up was 88 months. The Sillence classification was used to classify OI. Fifteen patients were classified as Type I; five as Type III and nine as Type IV. A total number of 245 procedures were recorded. Of these, 147 were surgical (pinning; intramedullary nailing and plating) while 98 were conservative ...
Osteogenesis imperfecta is one of the most commonly recognized inheritable disorders of the connecti...
Osteogenesis imperfecta is one of the most commonly recognized inheritable disorders of the connecti...
Osteogenesis imperfecta is a heritable condition characterized by abnormally brittle bones, with an ...
The aim of our study was to compare the surgical and conservative treatment of patients affected by ...
The aim of our study was to compare the surgical and conservative treatment of patients affected by ...
The aim of our study was to compare the surgical and conservative treatment of patients affected by ...
Introduction Osteogenesis imperfecta (OI) is a group of rare and relatively diverse genetic disorder...
Aim. Osteogenesis imperfecta (OI) is characterized by bone fragility and long bones deformities. Mos...
Osteogenesis imperfecta (OI) is a genetic disorder that is usually caused by disturbed production of...
Osteogenesis imperfecta (OI) or brittle bone disease, a heritable disorder of connective tissue, is ...
Osteogenesis imperfecta (OI), an inherited skeletal disorder characterized by low bone mass, bone fr...
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 ...
Background: Osteogenesis imperfect is a disease of genetic origin, which causes a defect in the form...
Ostegenesis imperfecta (OI) is a group of genetic diseases with a wide spectrum of severity, ranging...
Osteogenesis imperfecta is one of the most commonly recognized inheritable disorders of the connecti...
Osteogenesis imperfecta is one of the most commonly recognized inheritable disorders of the connecti...
Osteogenesis imperfecta is a heritable condition characterized by abnormally brittle bones, with an ...
The aim of our study was to compare the surgical and conservative treatment of patients affected by ...
The aim of our study was to compare the surgical and conservative treatment of patients affected by ...
The aim of our study was to compare the surgical and conservative treatment of patients affected by ...
Introduction Osteogenesis imperfecta (OI) is a group of rare and relatively diverse genetic disorder...
Aim. Osteogenesis imperfecta (OI) is characterized by bone fragility and long bones deformities. Mos...
Osteogenesis imperfecta (OI) is a genetic disorder that is usually caused by disturbed production of...
Osteogenesis imperfecta (OI) or brittle bone disease, a heritable disorder of connective tissue, is ...
Osteogenesis imperfecta (OI), an inherited skeletal disorder characterized by low bone mass, bone fr...
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 ...
Background: Osteogenesis imperfect is a disease of genetic origin, which causes a defect in the form...
Ostegenesis imperfecta (OI) is a group of genetic diseases with a wide spectrum of severity, ranging...
Osteogenesis imperfecta is one of the most commonly recognized inheritable disorders of the connecti...
Osteogenesis imperfecta is one of the most commonly recognized inheritable disorders of the connecti...
Osteogenesis imperfecta is a heritable condition characterized by abnormally brittle bones, with an ...