Meckel-Gruber syndrome
- PMID: 9579873
- DOI: 10.1007/s003810050198
Meckel-Gruber syndrome
Abstract
Meckel-Gruber syndrome is a congenital disorder characterized by occipital encephalocele, polydactyly and polycystic kidneys. This rare syndrome has been reported in the literature as incompatible with life. We present the case of a newborn afflicted with the clinical triad of Meckel-Gruber syndrome. Appropriate treatment instituted in our case led to a good early outcome.
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