A case report of recurrent Meckel Gruber syndrome / 대한산부인과학회지
Korean Journal of Obstetrics and Gynecology
;
: 2194-2198, 2006.
Artículo
en Coreano
| WPRIM
| ID: wpr-16768
ABSTRACT
Meckel Gruber syndrome consisting of an occipital encephalocele, polycystic kidney disease and polydactyly is a rare autosomal recessive disorder with a recurrence risk of 25%. Targeted ultrasonography in late embryonic or early fetal stages of pregnancy has great importance in diagnosis and management of affected pregnancy in high risk groups due to incomplete genetic mapping of meckel syndrome gene (MKS). We present a case of prenatal diagnosis at 14 weeks' gestational age of Meckel Gruber syndrome in a woman, who experienced same disorder in her previous pregnancy.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Diagnóstico Prenatal
/
Recurrencia
/
Ultrasonografía
/
Edad Gestacional
/
Polidactilia
/
Diagnóstico
/
Encefalocele
/
Enfermedades Renales Poliquísticas
Tipo de estudio:
Estudio diagnóstico
Límite:
Femenino
/
Humanos
/
Embarazo
Idioma:
Coreano
Revista:
Korean Journal of Obstetrics and Gynecology
Año:
2006
Tipo del documento:
Artículo
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