Child abuse and osteogenesis imperfecta: how can they be still misdiagnosed? A case report - D'Eufemia P, Palombaro M, Lodato V, Zambrano A, Celli M, Persiani P, De Bari MP, Sangiorgi L.

Osteogenesis imperfecta (OI) is a rare hereditary disease caused by mutations in genes coding for type I collagen, resulting in bone fragility. In literature are described forms lethal in perinatal period, forms which are moderate and slight forms where th...
Source: SafetyLit: All (Unduplicated) - Category: Global & Universal Tags: Age: Infants and Children Source Type: news