Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 2 de 2
Filtre
Ajouter des filtres








Gamme d'année
1.
Journal of the Korean Medical Association ; : 746-754, 1998.
Article Dans Coréen | WPRIM | ID: wpr-216621

Résumé

No abstract available.


Sujets)
Adolescent , Humains
2.
Korean Journal of Obstetrics and Gynecology ; : 198-202, 1997.
Article Dans Coréen | WPRIM | ID: wpr-172752

Résumé

Osteogenesis imperfecta is a relatively rare genetic condition of breakable bones with an incidence of 1 per 20,000~60,000. The clinical, genetic, and biochemical heterogeneity in osteogenesis imperfecta allows to least four subtypes to be distinguished. Prenatal diagnosis of osteogenesis imperfecta type II have been reported several times with ultrasonography. We recently experienced a case of osteogenesis imperfecta diagnosed in uterus by ultrasonogram and confirmed after termination and autopsy. We report here with a brief review of the literature.


Sujets)
Autopsie , Incidence , Ostéogenèse imparfaite , Ostéogenèse , Caractéristiques de la population , Diagnostic prénatal , Échographie , Utérus
SÉLECTION CITATIONS
Détails de la recherche