MECKEL GRUBER SYNDROME- A RARE CASE REPORT

<jats:p>Meckel Gruber Syndrome is a rare and lethal autosomal recessive congenital anomaly syndrome, characterized by a triad of : occipital encephalocele Postaxial polydactyly, bilateral dysplastic cystic kidneys and other occasional features. Diagnosis can be made on ultrasonography with atleast two of the major features. Here we present a pregnant women complicated with meckel gruber syndrome. We relayed on ultrasonography findings and MRI,preganancy was terminated at 22weeks of gestational age. Ultrasonography, MRI and clinical examination of bady after termination suggestive of Meckel Gruber Syndrome.</jats:p>