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Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1985 Oct;22(5):382–385. doi: 10.1136/jmg.22.5.382

Phenotypic variation in LADD syndrome.

E Thompson, M Pembrey, J M Graham
PMCID: PMC1049483  PMID: 4078868

Abstract

A mother and son are reported with chronic dacrocystitis, cup shaped ears, hearing loss, abnormal teeth, and poor formation of saliva and tears. They are similar to previously reported cases of lacrimo-auriculo-dento-digital (LADD) syndrome. The variability of expression of this autosomal dominant syndrome is discussed, and it is suggested that poor saliva and tear formation be added to the phenotype.

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Selected References

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

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