Oculodentodigital dysplasia and type III syndactyly: separate genetic entities or disease spectrum?
- 1 March 1990
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 27 (3), 169-175
- https://doi.org/10.1136/jmg.27.3.169
Abstract
A family is described with type III syndactyly and facies resembling the oculodentodigital dysplasia facial phenotype in the absence of any of the other characteristic findings of the latter condition. The relationship between type III syndactyly and oculodentodigital dysplasia is discussed.This publication has 10 references indexed in Scilit:
- Three new cases of oculodentodigital (ODD) syndrome: development of the facial phenotype.Journal of Medical Genetics, 1985
- The question of hypertelorism in oculodentoosseous dysplasiaAmerican Journal of Medical Genetics, 1981
- Oculodentodigital DysplasiaArchives of Ophthalmology (1950), 1979
- Familial translocation t(8;14) with a case of tertiary trisomy, +14q-.1978
- The Oculo-Dento-Digital Dysplasia Syndrome*American Journal of Ophthalmology, 1966
- Roentgen Differentiation of the Oculodentodigital Syndrome and the Hallermann-Streiff Syndrome in InfancyRadiology, 1966
- [The microphthalmos syndrome].1957
- SYNDACTYLY OF THE RING AND LITTLE FINGER1955
- A CASE OF SYNDACTYLISM OF THE RING AND LITTLE FINGERS1954
- THREE FURTHER CASES OF HEREDITARY DIGITAL ANOMALY SEEN IN THE OUT‐PATIENT DEPARTMENT OF GREAT ORMOND STREET HOSPITAL FOR SICK CHILDRENAnnals of Eugenics, 1931