Acrocallosal Syndrome (Schinzel Syndrome)

J Gordon Millichap

doi:10.15844/pedneurbriefs-2-3-2

Acrocallosal Syndrome (Schinzel Syndrome)

Pediatric Neurology Briefs

Volume 2 (1988): Issue 3

By: J Gordon Millichap

Open Access

|Mar 1988

Abstract

The acrocallosal syndrome, first described by Schinzel and characterized by dysmorphic features, macrocephaly, Polydactyly, mental retardation, and agenesis of the corpus callosum, is reported in two unrelated boys with consanguineous parents from the Centre de Génétique Médicale, Service de Pediatrie Générale and Radiologie, Hôpital d'Enfants de la Timone, Marseille, France.

References

Schinzel A Postaxial polydactyly, hallux duplication, absence of the corpus callosum, macrencephaly and severe mental retardation: a new syndrome? Helv Paediatr Acta 1979 May 34 2 141 6 457430
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Philip N Apicella N Lassman I Ayme S Mattei JF Giraud F The acrocallosal syndrome Eur J Pediatr 1988 Feb 147 2 206 8 10.1007/BF00442226 3366141
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-2-3-2 | Journal eISSN: 2166-6482

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Language: English

Page range: 17 - 18

Published on: Mar 1, 1988

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Acrocallosal Syndrome,

Dysmorphic Features,

Schinzel Syndrome

© 1988 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 2 (1988): Issue 3