Autosomal recessive syndrome characterized by hypogenesis or agenesis of CORPUS CALLOSUM. Clinical features include MENTAL RETARDATION; CRANIOFACIAL ABNORMALITIES; digital malformations, and growth retardation.
Synonyms: Acrocallosal Syndrome, Acrocallosal Syndromes, Hallux Duplication, Postaxial Polydactyly, and Absence of Corpus Callosum, Syndromes, Acrocallosal, Syndrome, Acrocallosal
Instance information
comment
2009
identifier
D055673