Meckel-Gruber syndrome is a congenital disorder characterized by occip
ital encephalocele, polydactyly and polycystic kidneys. This rare synd
rome has been reported in the literature as incompatible with life. We
present the case of a newborn afflicted with the clinical triad of Me
ckel-Gruber syndrome. Appropriate treatment instituted in our case led
to a good early outcome.