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Ceylon Med J ; 2004 Mar; 49(1): 30-1
Article in English | IMSEAR | ID: sea-47389

ABSTRACT

Meckel Gruber syndrome is an uncommon, lethal, autosomal recessive disorder, associated consistently with polycystic kidneys, posterior encephalocoele and polydactly. We report three cases in non-consanguineous marriages, suggesting that the single gene defect occurs more commonly in non-consanguineous marriages than mutant genes associated with other autosomal recessive disorders that are usually related with consanguineous marriages. The usefulness of prenatal diagnosis is discussed.


Subject(s)
Abnormalities, Multiple/genetics , Consanguinity , Encephalocele/genetics , Female , Fetal Death/genetics , Humans , Infant, Newborn , Male , Polycystic Kidney Diseases/genetics , Polydactyly/genetics , Syndrome
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