Abstract

We present a case of a 1-day-old neonate with classical findings of acrocallosal syndrome. The child presented with difficulty in feeding. Clinically, the patient had craniofacial anomalies and digital malformations. Imaging with ultrasonography and magnetic resonance imaging revealed characteristic features of corpus callosum agenesis with dandy walker malformation. A classical case of acrocallosal syndrome with sporadic occurrence is discussed with a detailed review of all such previously reported cases in the literature till date and a discussion of possible differentials.

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