Korean J Obstet Gynecol.  2001 May;44(5):1004-1007.

A Case of Meckel-Gruber Syndrome Diagnosed by Ultrasonography at 18 Weeks` Gestation

Affiliations
  • 1Department of Obstetrics and Gynecology, College of Medicine, Yonsei University, Seoul, Korea.

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.

Keyword

Meckel-Gruber syndrome; Prenatal diagnosis; Ultrasonography

MeSH Terms

Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Encephalocele
Liver
Multicystic Dysplastic Kidney
Polydactyly
Pregnancy*
Prenatal Diagnosis
Ultrasonography*
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