| Literature DB >> 2166860 |
J Wendisch1, P Lorenz, M Kabus, E Rupprecht, S Walther.
Abstract
The acrocallosal syndrome is a rare congenital malformation syndrome with the main findings: agenesis of the corpus callosum, craniofacial dysmorphisms, mental retardation, polydactyly of the hands and/or feet. We report a patient with partial agenesis of the corpus callosum, dolichocephalus, broad and short nose, low-set and posteriorly rotated ears, pre- and postaxial polydactyly of feet, duplication with syndactyly of big toes, and postaxial hexadactyly of the left hand. Differential diagnosis and the genetic counseling are discussed.Entities:
Mesh:
Year: 1990 PMID: 2166860
Source DB: PubMed Journal: Kinderarztl Prax ISSN: 0023-1495