Publications by authors named "Mohamed Emad El-Dein Hemdan"
Background: Osteogenesis imperfecta (OI) is a genetic connective tissue disease defined by the loss of bone mass and density, which makes the bones more brittle and more likely to fracture over time. Bone deformity and articular instability are the subsequent symptoms.
Case Report: This 25-year-old man had malformed lower limbs and trouble walking due to OI and dwarfism.