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Corpus callosum agenesis in Coffin-Lowry syndrome
1Centre for Human Genetics, University of Leuven, Belgium.
Abstract:
We describe a boy with the syndrome of Coffin-Lowry whose CT-scan showed corpus callosum agenesis. Follow-up data are given and diagnostic considerations are discussed. A review is given of the CNS-malformations so far reported in patients with the syndrome of Coffin-Lowry.
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