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Mid-portion agenesis of corpus callosum in a presumed Baller-Gerold syndrome.

作者信息

Dunac A, Van Bogaert P, David P, Avni E F, Paduart O, Szliwowski H B, Van Regemorter N

机构信息

Department of Neurology (Pediatric Neurology), Hôpital Erasme, Université Libre de Bruxelles, Belgium.

出版信息

Neuropediatrics. 1995 Oct;26(5):273-5. doi: 10.1055/s-2007-979772.

Abstract

We report an association of trigonocephaly and thumb hypoplasia in a 6.5-year-old boy, diagnosed as Baller-Gerold syndrome. In addition to craniosynostosis and radial limb defect, which are constant in this syndrome, our patient presents two unusual features: the first is an epidermal nevus and the second is an agenesis of the middle portion of corpus callosum. This unique type of callosal agenesis in the context of a polymalformative disorder supports the hypothesis that partial agenesis of corpus callosum may be due to an event occurring before the 12th week gestation with continued development of the midline structures.

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