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OSTEOGENESIS IMPERFECTA IN PREGNANCY: CASE REPORT

机译:妊娠骨不全症:病例报告

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Osteogenesis imperfecta is a rare inherited Connective tissue disorder with an expression that varies from mild to severe disease affecting bone, Sclera and middle ear. Fertility is preserved, especially in those patients with type 1. We present hereby a pregnant woman with Osteogenesis imperfecta that had over 30 fractures in long bones and vertebrae. The object of this report was to determine choice of delivery method, maternal and neonatal Complications and prenatal diagnosis.
机译:成骨不全症是一种罕见的遗传性结缔组织疾病,其表达范围从轻度到严重,影响到骨骼,巩膜和中耳。生育力得以保留,尤其是对于那些1型患者。我们特此为一名成骨不全孕妇,其长骨和椎骨骨折超过30处。本报告的目的是确定分娩方法,母婴并发症和产前诊断的选择。

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