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Meckel Gruber Syndrome- A Rare Case Report
2022
Journal:  
International Journal of Advanced Research
Author:  
Abstract:

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.

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International Journal of Advanced Research

Field :   Sosyal, Beşeri ve İdari Bilimler

Journal Type :   Uluslararası

Metrics
Article : 10.413
Cite : 722
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