We report on a girl presenting with mental retardation, craniofacial dysmorphisms, and syndactyly. The child's mother and maternal grandfather presented bilateral syndactyly of toes 2 and 3. These manifestations, falling within the ambit of what has been termed the craniodigital syndromes, were first reported by Scott et al (1971) in 3 brothers.
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Soekarman D. , Volcke P., Fryns JPOn the nosology of the craniodigital syndromes: report of a family and review of the literature. Genet Couns . 1997;8:217-222.
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