We report the clinical and cytogenetic data on seven members of a family, spaning three generations, who showed congenital facial diplegia and finger contractures. Each affected member showed an identical chromosome abnormality, reciprocal translocation between chromosome 1 and 13. The concurrence of the clinical and cytogenetic defect in this family suggests a direct and possibly etiologic relationship.

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A CROSS-SECTIONAL, controlled study of 40 families, one member each of which presented with focal "temporal lobe" epilepsy, has been described.

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