A Case of Perinatal Lethal Osteogeenesis Imperfecta / 대한주산의학회잡지
Korean Journal of Perinatology
;
: 55-59, 1997.
Artículo
en Coreano
| WPRIM
| ID: wpr-100469
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.
Texto completo:
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Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Osteogénesis Imperfecta
/
Esclerótica
/
Ultrasonografía
/
Tejido Conectivo
/
Dentición
/
Fracturas Óseas
/
Pérdida Auditiva
Tipo de estudio:
Estudio diagnóstico
Idioma:
Coreano
Revista:
Korean Journal of Perinatology
Año:
1997
Tipo del documento:
Artículo
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