Meckel-Gruber Syndrome with Lingual Cyst
Shalu Gupta, S Basu, Ashok Kumar, B D Bhatia
Division of Neonatology, Department of Pediatrics, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India
Abstract

Meckel Gruber syndrome is a rare autosomal disorder characterized by encephalocele, polycystic kidneys, and polydactyly. The diagnosis is possible antenatally. We report a case of Meckel Gruber syndrome with a recurrence of cranium bifidum. We also found an associated posterior lingual cyst. This association is not reported earlier.
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