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A Case of Perinatal Lethal Osteogeenesis Imperfecta / 대한주산의학회잡지
Article in Ko | WPRIM | ID: wpr-100469
Responsible library: WPRO
ABSTRACT
Osteogenesis imperfecta is a rare congenital disease. It is a heterogeneous group of inherited disorders characterized by multiple bone fracture, blue sclera, hearing loss, abnormalities of dentition and widespread connective tissue ahnormality. We experienced a case of osteogenesis imperfecta diagnosed in utero by ultrasonogram and confirmed hy postnatal radiograph after delivery. We present the case with a hrief review of the literature.
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Full text: 1 Index: WPRIM Main subject: Osteogenesis Imperfecta / Sclera / Ultrasonography / Connective Tissue / Dentition / Fractures, Bone / Hearing Loss Type of study: Diagnostic_studies Language: Ko Journal: Korean Journal of Perinatology Year: 1997 Type: Article
Full text: 1 Index: WPRIM Main subject: Osteogenesis Imperfecta / Sclera / Ultrasonography / Connective Tissue / Dentition / Fractures, Bone / Hearing Loss Type of study: Diagnostic_studies Language: Ko Journal: Korean Journal of Perinatology Year: 1997 Type: Article