A Case of Edward Syndrome / 대한산부인과학회잡지
Korean Journal of Obstetrics and Gynecology
;
: 2155-2160, 2001.
Artículo
en Coreano
| WPRIM
| ID: wpr-99343
ABSTRACT
Trisomy 18, called Edward syndrome, occurs in about 3500-8000 births. It is much more common at conception, with about 95% of cases resulting in spontaneous abortion or stillbirth. Postnatal survival is poor, with the majority of patients dying in early infancy. Characteristic findings include cardiac malformations, mental retardation, growth retardation, a prominent occiput, micrognathia, clenched hands, and rocker-bottom feet, omphalocele. The prenatal sonographic findings of our case include delayed growth, omphalocele, wrist joint fixation, choroid plexus cyst, hydramnios and postnatal gross findings include growth retardation, omphalocele, wirst joint fixation, absence of radius, syndactyly, focal absence of phalanges and flexion deformities of fingers and toes. We report a case of prenatally diagnosed Edward syndrome, which is confirmed by chromosome analysis, with brief review of related literatures.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Radio (Anatomía)
/
Anomalías Congénitas
/
Trisomía
/
Articulación de la Muñeca
/
Dedos del Pie
/
Aborto Espontáneo
/
Plexo Coroideo
/
Ultrasonografía Prenatal
/
Polihidramnios
/
Ultrasonografía
Tipo de estudio:
Estudio diagnóstico
Límite:
Femenino
/
Humanos
/
Embarazo
Idioma:
Coreano
Revista:
Korean Journal of Obstetrics and Gynecology
Año:
2001
Tipo del documento:
Artículo
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