Literature DB >> 2166860

[The acrocallosal syndrome. Report of an additional case].

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.

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Year:  1990        PMID: 2166860

Source DB:  PubMed          Journal:  Kinderarztl Prax        ISSN: 0023-1495


  1 in total

1.  A family with one child with acrocallosal syndrome, one child with anencephaly-polydactyly, and parental consanguinity.

Authors:  S Cataltepe; E Tuncbilek
Journal:  Eur J Pediatr       Date:  1992-04       Impact factor: 3.183

  1 in total

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