Abstract
We report an exceedingly rare case of megalencephaly, postaxial polydactyly, polymicrogyria, and hydrocephalus in a 9-monthold infant. The information in the article will help doctors to perform adequate differential diagnostic search in time. We describe the history of this syndrome discovery and provide a detailed description of the results of magnetic resonance imaging Key words: congenital abnormalities of the central nervous system, hydrocephalus, megalencephaly, perinatal diagnosis, fetus, polymicrogyria, postaxial polydactyly
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