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Korean Journal of Perinatology ; : 55-59, 1997.
Artigo em Coreano | WPRIM | ID: wpr-100469

RESUMO

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.


Assuntos
Tecido Conjuntivo , Dentição , Fraturas Ósseas , Perda Auditiva , Osteogênese Imperfeita , Esclera , Ultrassonografia
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