[Acardiac malformation: ultrasonographic diagnosis. A case report]. / Le monstre acardiaque: diagnostic échographique. A propos d'un cas.
Rev Fr Gynecol Obstet
; 88(4): 267-72, 1993 Apr.
Article
en Fr
| MEDLINE
| ID: mdl-8502900
Acardia is an extremely rare malformation which is seen in less than 1 per cent of monozygous twin pregnancies. Pathological aspects and etiopathogenic theories concerning this malformation are reviewed on the basis of a case diagnosed in utero at 24 weeks. The value of the antenatal diagnosis of this malformation is that of monitoring the progression of the pregnancy and predicting the fate of the healthy twin.
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Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Gemelos Monocigóticos
/
Ultrasonografía Prenatal
/
Cardiopatías Congénitas
Tipo de estudio:
Diagnostic_studies
/
Prognostic_studies
Límite:
Adult
/
Female
/
Humans
/
Newborn
/
Pregnancy
Idioma:
Fr
Revista:
Rev Fr Gynecol Obstet
Año:
1993
Tipo del documento:
Article
País de afiliación:
Túnez
Pais de publicación:
Francia