Korean J Obstet Gynecol.  2006 Oct;49(10):2194-2198.

A case report of recurrent Meckel Gruber syndrome

Affiliations
  • 1Department of Obstetrics and Gynecology, College of Medicine, Chungnam National University, Daejeon, Korea. rheyun@cnu.ac.kr

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.

Keyword

Meckel Gruber syndrome; Prenatal diagnosis; Ultrasonography

MeSH Terms

Diagnosis
Encephalocele
Female
Gestational Age
Humans
Polycystic Kidney Diseases
Polydactyly
Pregnancy
Prenatal Diagnosis
Recurrence
Ultrasonography
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