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Family experience with osteogenesis imperfecta type 1: the most distressing sit...

Santos, Margarida Custódio dos; Pires, Ana Filipa; Soares, Kelly; Barros, Luísa

Background: Osteogenesis imperfecta (OI) is a rare genetic disorder characterized by decreased bone mass and increased bone fragility. Despite increasing research on the biomedical aspects of the disease, only a few studies focus on the psychosocial implications of living with OI. This study aimed to explore the situations that are perceived by OI type-1 children, their parents, and siblings, as being the most ...

Date: 2018   |   Origin: Repositório Científico do Instituto Politécnico de Lisboa
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