Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1985 Oct;22(5):386–389. doi: 10.1136/jmg.22.5.386

Three new cases of oculodentodigital (ODD) syndrome: development of the facial phenotype.

M A Patton, K M Laurence
PMCID: PMC1049484  PMID: 3935793

Abstract

Three new cases of oculodentodigital (ODD) syndrome are reported. The clinical features are discussed and the development of the characteristic facial appearance is illustrated. Conductive deafness is reported in one of our cases and has been reported in six previous cases. It is suggested that it is a feature of the syndrome which is amenable to treatment.

Full text

PDF
388

Images in this article

Selected References

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

  1. Eidelman E., Chosack A., Wagner M. L. Orodigitofacial dysostosis and oculodentodigital dysplasia. Two distinct syndromes with some similarities. Oral Surg Oral Med Oral Pathol. 1967 Mar;23(3):311–319. doi: 10.1016/0030-4220(67)90141-7. [DOI] [PubMed] [Google Scholar]
  2. Fará M., Gorlin R. J. The question of hypertelorism in oculodentoosseous dysplasia. Am J Med Genet. 1981;10(1):101–102. doi: 10.1002/ajmg.1320100112. [DOI] [PubMed] [Google Scholar]
  3. GILLESPIE F. D. A HEREDITARY SYNDROME: "DYSPLASIA OCULODENTODIGITALIS. Arch Ophthalmol. 1964 Feb;71:187–192. doi: 10.1001/archopht.1964.00970010203009. [DOI] [PubMed] [Google Scholar]
  4. GORLIN R. J., MISKIN L. H., St GEME J. W. Oculodentodigital dysplasia. J Pediatr. 1963 Jul;63:69–75. doi: 10.1016/s0022-3476(63)80304-2. [DOI] [PubMed] [Google Scholar]
  5. Jones K. L., Smith D. W., Harvey M. A., Hall B. D., Quan L. Older paternal age and fresh gene mutation: data on additional disorders. J Pediatr. 1975 Jan;86(1):84–88. doi: 10.1016/s0022-3476(75)80709-8. [DOI] [PubMed] [Google Scholar]
  6. Judisch G. F., Martin-Casals A., Hanson J. W., Olin W. H. Oculodentodigital dysplasia. Four new reports and a literature review. Arch Ophthalmol. 1979 May;97(5):878–884. doi: 10.1001/archopht.1979.01020010436007. [DOI] [PubMed] [Google Scholar]
  7. Kurlander G. J., Lavy N. W., Campbell J. A. Roentgen differentiation of the oculodentodigital syndrome and the Hallermann-Streiff syndrome in infancy. Radiology. 1966 Jan;86(1):77–86. doi: 10.1148/86.1.77. [DOI] [PubMed] [Google Scholar]
  8. MEYER-SCHWICKERATH G., GRUTERICH E., WEYERS H. Mikrophthalmussyndrome. Klin Monbl Augenheilkd Augenarztl Fortbild. 1957;131(1):18–30. [PubMed] [Google Scholar]
  9. Reisner S. H., Kott E., Bornstein B., Salinger H., Kaplan I., Gorlin R. J. Oculodentodigital dysplasia. Am J Dis Child. 1969 Oct;118(4):600–607. doi: 10.1001/archpedi.1969.02100040602013. [DOI] [PubMed] [Google Scholar]
  10. Thodén C. J., Ryöppy S., Kuitunen P. Oculodentodigital dysplasia syndrome. Report of four cases. Acta Paediatr Scand. 1977 Sep;66(5):635–638. doi: 10.1111/j.1651-2227.1977.tb07960.x. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES