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Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1983 Dec;20(6):433–435. doi: 10.1136/jmg.20.6.433

Syndrome of polydactyly, cleft lip, lingual hamartomas, renal hypoplasia, hearing loss, and psychomotor retardation: variant of the Mohr syndrome or a new syndrome?

J F Mattei, S Aymé
PMCID: PMC1049175  PMID: 6686259

Abstract

Three sibs, the proband and two monozygotic twins, have a condition including mental retardation, postnatal somatic retardation, preaxial polydactyly of the feet, bifid third metacarpal, median cleft lip, fatty hamartomas on the dorsum of the tongue, conductive hearing loss, and unilateral or bilateral renal agenesis. This probably autosomal recessive syndrome could be a further example of the condition described by Váradi et al or a variant of the Mohr syndrome.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Baraitser M., Burn J., Fixsen J. A female infant with features of Mohr and Majewski syndromes: variable expression, a genetic compound, or a distinct entity? J Med Genet. 1983 Feb;20(1):65–67. doi: 10.1136/jmg.20.1.65. [DOI] [PMC free article] [PubMed] [Google Scholar]
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