The authors present a case of Osteogenesis Imperfecta, emphasizing the clinical and epidemiological characteristics, forms of classification and treatment of the disease. This is an important case not only to the knowledge of pediatricians and orthopedists, but also for other professionals involved with the problem. This article has been jointly described by the Departments of Pediatrics and Neonatology of the Girassol Clinic in Luanda Capital of the Republic of Angola, Africa
Study of 16 patients with Type Ill osteogenesis imperfecta showed marked elongation of the pedicles ...
A description is made of the pathological findings of two fetuses affected by lethal congenital ost...
Osteogenesis imperfecta is a genetic disorder by bone fragility and decreased bone density. Ligament...
Osteogenesis imperfecta (OI) is a rare disease with a wide spectrum of clinical and genetic variabil...
Osteogenesis imperfecta, innate brittle bone disease, is a very serious disease. It is inheritable d...
Osteogenesis imperfecta (OI), an inherited skeletal disorder characterized by low bone mass, bone fr...
Osteogenesis imperfecta is an inherited disorder of the connective tissue. The extreme bone fragilit...
Osteogenesis imperfecta (OI) is a metabolic bone disorder commonly encountered in orthopaedic practi...
Osteogenesis Imperfecta (OI) is an uncommon congenital abnormality of the connective tissues in whic...
ABSTRACT Background: Osteogenesis imperfecta (OI) comprises a heterogeneous group of diseases charac...
Osteogenesis imperfecta is a heterogeneous group of connective tissue disorders; it is characterized...
Osteogenesis imperfecta (OI) is an extremely rare congenital anomaly with similarities to various co...
The Osteogenesis imperfecta (OI) is a rare genetic disorder characterized by bone fragility and oste...
Osteogenesis imperfecta (OI) is the most frequent hereditary bone disease during childhood. In most ...
Wstęp: Wrodzona łamliwość kości to grupa genetycznie uwarunkowanych chorób, charakteryzująca się głó...
Study of 16 patients with Type Ill osteogenesis imperfecta showed marked elongation of the pedicles ...
A description is made of the pathological findings of two fetuses affected by lethal congenital ost...
Osteogenesis imperfecta is a genetic disorder by bone fragility and decreased bone density. Ligament...
Osteogenesis imperfecta (OI) is a rare disease with a wide spectrum of clinical and genetic variabil...
Osteogenesis imperfecta, innate brittle bone disease, is a very serious disease. It is inheritable d...
Osteogenesis imperfecta (OI), an inherited skeletal disorder characterized by low bone mass, bone fr...
Osteogenesis imperfecta is an inherited disorder of the connective tissue. The extreme bone fragilit...
Osteogenesis imperfecta (OI) is a metabolic bone disorder commonly encountered in orthopaedic practi...
Osteogenesis Imperfecta (OI) is an uncommon congenital abnormality of the connective tissues in whic...
ABSTRACT Background: Osteogenesis imperfecta (OI) comprises a heterogeneous group of diseases charac...
Osteogenesis imperfecta is a heterogeneous group of connective tissue disorders; it is characterized...
Osteogenesis imperfecta (OI) is an extremely rare congenital anomaly with similarities to various co...
The Osteogenesis imperfecta (OI) is a rare genetic disorder characterized by bone fragility and oste...
Osteogenesis imperfecta (OI) is the most frequent hereditary bone disease during childhood. In most ...
Wstęp: Wrodzona łamliwość kości to grupa genetycznie uwarunkowanych chorób, charakteryzująca się głó...
Study of 16 patients with Type Ill osteogenesis imperfecta showed marked elongation of the pedicles ...
A description is made of the pathological findings of two fetuses affected by lethal congenital ost...
Osteogenesis imperfecta is a genetic disorder by bone fragility and decreased bone density. Ligament...