Abstract
We reported a case of two days old baby with typical features of Acrocallosal syndrome. The characteristic features of this syndrome are craniofacial abnormalities, distinctive digital malformation and corpus callosum hypoplasia/agenesis. USG cranium and NECT of brain reveals characteristic features of corpus callosum agenesis and posterior fossa arachnoid cyst.
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More From: Journal of Evolution of Medical and Dental Sciences
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