Meckel-Gruber syndrome: a case report with review of literature.
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Date
2015-02
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Abstract
Meckel Gruber syndrome is an autosomal recessive disorder, characterized by a combination of renal cysts or cystic renal dysplasia, developmental anomalies of the central nervous system, hepatic dysgenesis and polydactyly. It is a rare syndrome with highest incidence in Gujarati Indians and Finnish population. We report a case of Meckel Gruber syndrome in non Gujarati Indian which was diagnosed on fetal autopsy.
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Keywords
Meckel-Gruber syndrome, Rare, Non Gujarati Indian
Citation
Prasad Usha, Prasad Uma, Sushma J, Lakshmi A Bhagya. Meckel-Gruber syndrome: a case report with review of literature. International Journal of Research in Medical Sciences. 2015 Feb; 3(2): 484-487.