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Split-foot anomaly, microphthalmia, cleft-lip and cleft-palate, and mental retardation associated with a chromosome 6;13 translocation.
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1993
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GeneticsPathologyDermatologyMendelian DisorderCongenital DisordersCraniofacial DevelopmentCraniofacial AnomaliesChromosome 6Central Cleft-lipMental RetardationChromosome 9NeurogeneticsCleft LipDown SyndromeSplit-hand/split-foot AnomalyDevelopmental AnomalyThumb HypoplasiaDevelopmental BiologyGenetic DisorderMedicineCraniofacial DisorderSplit-foot Anomaly
The split-hand/split-foot anomaly is a component of several disorders which may occur sporadically or be transmitted as autosomal dominant or autosomal recessive traits. We describe a severely mentally handicapped patient with ectrodactyly of both feet in association with extreme microphthalmia, central cleft-lip and palate and mental retardation. She has an apparent de novo 46,XX,t(6;13) (q21;q12) unbalanced translocation. Either of these breakpoints may be the locus for the ectrodactyly-ectodermal dysplasia-facial cleft (EEC) syndrome.