Cole D E
Department of Pediatrics and Pathology, Dalhousie University, Halifax, Nova Scotia, Canada.
Am J Med Genet. 1993 Jan 15;45(2):207-11. doi: 10.1002/ajmg.1320450211.
Osteogenesis imperfecta (OI) is an inherited disorder in which affected individuals are stigmatized by virtue of physical differences from their peers. The extent to which these differences alter life style depend on the severity of the disorder, its natural history, the extent to which it affects social integration, the effect on physical appearance, and the presence of other affected family members. Some of these factors may adversely influence the ability of affected individuals to effectively adjust to their social and work environment and recognition of these factors may aid individuals and helpers in easing the path to a constructive life.
成骨不全症(OI)是一种遗传性疾病,患者因与同龄人存在身体差异而受到歧视。这些差异对生活方式的影响程度取决于疾病的严重程度、其自然病史、对社会融合的影响程度、对外表的影响以及其他受影响家庭成员的情况。其中一些因素可能会对患者有效适应社会和工作环境的能力产生不利影响,认识到这些因素可能有助于患者及其帮助者顺利走向建设性的生活。