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  • Title: Acrocallosal syndrome: a new case.
    Author: Lungarotti MS, Marinelli D, Mezzetti D, Caputo N, Calabro A.
    Journal: Am J Med Genet; 1991 Jul 01; 40(1):94-6. PubMed ID: 1887856.
    Abstract:
    We describe a 2-month-old infant girl with typical clinical manifestations of the acrocallosal syndrome: characteristic face, agenesis of corpus callosum, polydactyly associated with other anomalies of the extremities, and mental retardation. The importance of a correct nosology and genetic counseling is underlined on the basis of the description of familiar cases of the syndrome.
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