A Case of Osteogenesis Imperfecta: Diagnosed in Uterus by Ultrasonogram / 대한산부인과학회잡지
Korean Journal of Obstetrics and Gynecology
;
: 198-202, 1997.
Artículo
en Coreano
| WPRIM
| ID: wpr-172752
ABSTRACT
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.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Osteogénesis
/
Osteogénesis Imperfecta
/
Diagnóstico Prenatal
/
Autopsia
/
Útero
/
Características de la Población
/
Incidencia
/
Ultrasonografía
Tipo de estudio:
Estudio diagnóstico
/
Estudio de incidencia
/
Estudio pronóstico
Idioma:
Coreano
Revista:
Korean Journal of Obstetrics and Gynecology
Año:
1997
Tipo del documento:
Artículo
Similares
MEDLINE
...
LILACS
LIS