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

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.
     Advertisements by :    Septilin by Himalaya Mega-CV by Aristo
Disclaimer: The information given by is provided by medical and paramedical & Health providers voluntarily for display & is meant only for informational purpose. The site does not guarantee the accuracy or authenticity of the information. Use of any information is solely at the user's own risk. The appearance of advertisement or product information in the various section in the website does not constitute an endorsement or approval by Pediatric Oncall of the quality or value of the said product or of claims made by its manufacturer.
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.