A Case of Meckel-Gruber Syndrome Diagnosed by Ultrasonography at 18 Weeks` Gestation / 대한산부인과학회잡지
Korean Journal of Obstetrics and Gynecology
;
: 1004-1007, 2001.
Article
in Korean
| WPRIM
| ID: wpr-98011
ABSTRACT
Meckel-Gruber syndrome is a congenital disorder characterized by occipital encephalocele, bilateral multicystic kidneys with fibrotic changes of the liver and postaxial polydactyly. Other anomalies are frequently associated. This syndrome is a rare autosomal recessive disorder often resulting in neonatal death within a few hours of life and has the high recurrence(one in four) in future pregnancies. We present the case of Meckel-Gruber syndrome diagnosed by ultrasonography at 18 weeks` gestation with a brief literature review.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Prenatal Diagnosis
/
Ultrasonography
/
Polydactyly
/
Multicystic Dysplastic Kidney
/
Encephalocele
/
Liver
/
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Type of study:
Diagnostic study
Limits:
Pregnancy
Language:
Korean
Journal:
Korean Journal of Obstetrics and Gynecology
Year:
2001
Type:
Article
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