Gulati, SheffaliMenon, ShajiKabra, MadhulikaKalra, Veena2003-02-292009-05-302003-02-292009-05-302003-02-29Gulati S, Menon S, Kabra M, Kalra V. Schinzel acrocallosal syndrome. Indian Journal of Pediatrics. 2003 Feb; 70(2): 173-6http://imsear.searo.who.int/handle/123456789/78922Acrocallosal syndrome (ACLS), also known by its synonyms: Schinzel Acrocallosal syndrome and Hallux duplication, Postaxial polydactyly and absence of corpus callosum, is a rare genetic disorder that is apparent at birth. Although autosomal recessive inheritence has been suggested, ACLS often appears to occur sporadically. Typical characteristics of ACLS are hypoplasia/agenesis of corpus callosum, moderate to severe mental retardation, characteristic craniofacial abnormalities, distinctive digital malformations and growth retardation. It has not been reported from India so far. This article reports a 5-month-old boy with combination of abnormalities consistent with acrocallosal syndrome.engAbnormalities, Multiple --geneticsCorpus Callosum --abnormalitiesHumansInfantMalePolydactyly --geneticsSeizures --etiologySyndromeCase Reports