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Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1993 Oct;30(10):870–872. doi: 10.1136/jmg.30.10.870

Orofaciodigital syndrome type III in two sibs.

R A Smith 1, D Gardner-Medwin 1
PMCID: PMC1016572  PMID: 8230165

Abstract

A brother and sister with mental retardation, malformations of the cerebellar vermis, characteristic 'metronome' eye movements, lingual hamartomas, and postaxial polydactyly are described. The clinical overlap with the OFD group of syndromes, in particular OFD III and OFD VI, and Joubert's syndrome is discussed. If OFD III syndrome is to be recognised as a distinct entity, these two cases represent the second and third cases reported.

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Selected References

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