Neurosurgical implications of osteogenesis imperfecta in a child after fall: case illustration - Moscote-Salazar LR, Koller O, Valenzuela S, Narvaez-Rojas A, Satyarthee GD, Mo-Carrascal J, Maraby J.

Osteogenesis imperfecta (OI) is a group of hereditary genetic pathologies of connective tissue, which is characterized by bone fragility and fractures. It is classified into types I, II, III, IV, V, and VI. The disorder is caused by an autosomal-dominant m...
Source: SafetyLit - Category: International Medicine & Public Health Tags: Age: Infants and Children Source Type: news