Carpenter’s syndrome: A rare craniofacial dysmorphic syndrome

Sir,We report a case of carpenter's syndrome in a child ofconsanguineous marriage. The child was having cleft lipand turricephaly, polydactyly in both hands, polydactylyand syndactyly in lower limbs. (Fig. 1). The patient wasevaluated with MRI. T1W axial view MRI was showingcortical atrophy, corpus callosum agenesis, and in sagitalview tower shaped skull, and ventricles seem to be singledue to cortical atrophy (Fig. 2). There was no cardiacanomaly on echocardiography.