ABSTRACT Background: Osteogenesis imperfecta (OI) comprises a heterogeneous group of diseases characterized by susceptibility to bone fractures with variable severity and, in most cases, with presumed or proven defects in collagen type I biosynthesis and an estimated prevalence of 1/15,000 births. Management is multidisciplinary involving mainly surgery, physiotherapy, and rehabilitation Case Presentation: A young woman the age of 19 years old came to the Endocrine Polyclinic of H. Adam Malik Hospital, with a complaint of a fracture of the arm and left thigh for 4 years due to a slip. Since a small age, there was difficulty walking due to the twisted bones of the limbs, and surgery was performed. The conclusion of X-ray of right and left fe...
Osteogenesis imperfecta (OI), an inherited skeletal disorder characterized by low bone mass, bone fr...
Osteogenesis imperfecta (OI) is a rare hereditary disease caused by mutations in genes coding for ty...
Osteogenesis imperfecta (OI) is a rare disease with a wide spectrum of clinical and genetic variabil...
Osteogenesis Imperfecta (OI) is an uncommon congenital abnormality of the connective tissues in whic...
Osteogenesis imperfecta (OI) is a connective tissue disorder that is caused by genetic mutation. OI ...
Osteogenesis imperfecta is an inherited connective tissue disorder with wide phenotypic and molecula...
Osteogenesis imperfecta (OI) or brittle bone disease, a heritable disorder of connective tissue, is ...
Osteogenesis imperfecta is an inherited connective tissue disorder with wide phenotypic and molecula...
Osteogenesis imperfecta (OI) is a metabolic bone disorder commonly encountered in orthopaedic practi...
Osteogenesis imperfecta (OI) is a group of rare inherited disorders of connective tissue with the ha...
Osteogenesis imperfecta (OI) is an uncommon genetic bone disease associated with brittle bones and f...
Osteogenesis imperfecta (OI), or brittle bone disease, is a heterogeneous disorder characterised by ...
A 14 months -old male patient is brought to the outpatient clinic with a history of multiple bone fr...
Osteogenesis imperfecta (OI) is a heterogeneous heritable connective tissue disorder characterized b...
Osteogenesis imperfecta or brittle bone disease, a heritable disorder of connective tissue, is the m...
Osteogenesis imperfecta (OI), an inherited skeletal disorder characterized by low bone mass, bone fr...
Osteogenesis imperfecta (OI) is a rare hereditary disease caused by mutations in genes coding for ty...
Osteogenesis imperfecta (OI) is a rare disease with a wide spectrum of clinical and genetic variabil...
Osteogenesis Imperfecta (OI) is an uncommon congenital abnormality of the connective tissues in whic...
Osteogenesis imperfecta (OI) is a connective tissue disorder that is caused by genetic mutation. OI ...
Osteogenesis imperfecta is an inherited connective tissue disorder with wide phenotypic and molecula...
Osteogenesis imperfecta (OI) or brittle bone disease, a heritable disorder of connective tissue, is ...
Osteogenesis imperfecta is an inherited connective tissue disorder with wide phenotypic and molecula...
Osteogenesis imperfecta (OI) is a metabolic bone disorder commonly encountered in orthopaedic practi...
Osteogenesis imperfecta (OI) is a group of rare inherited disorders of connective tissue with the ha...
Osteogenesis imperfecta (OI) is an uncommon genetic bone disease associated with brittle bones and f...
Osteogenesis imperfecta (OI), or brittle bone disease, is a heterogeneous disorder characterised by ...
A 14 months -old male patient is brought to the outpatient clinic with a history of multiple bone fr...
Osteogenesis imperfecta (OI) is a heterogeneous heritable connective tissue disorder characterized b...
Osteogenesis imperfecta or brittle bone disease, a heritable disorder of connective tissue, is the m...
Osteogenesis imperfecta (OI), an inherited skeletal disorder characterized by low bone mass, bone fr...
Osteogenesis imperfecta (OI) is a rare hereditary disease caused by mutations in genes coding for ty...
Osteogenesis imperfecta (OI) is a rare disease with a wide spectrum of clinical and genetic variabil...