Oculodentodigital dysplasia
- 1 January 1982
- journal article
- research article
- Published by Taylor & Francis in Ophthalmic Paediatrics and Genetics
- Vol. 1 (3) , 227-231
- https://doi.org/10.3109/13816818209036037
Abstract
A five-year-old boy showed a typical oculodentodigital dysplasia (microphthalmos, microcornea, abnormal texture of the iris, corectopia, persistent pupillary membrane, cataract, short palpebral fissures and epicanthal folds). the ERG and VER were extinguished. Echography revealed a bilateral persistent hyperplastic primary vitreous. the cases of the literature are reviewed. In none of them this congenital anomaly was mentioned.This publication has 3 references indexed in Scilit:
- DOMINANT ACROCEPHALOSYNDACTYLYHereditas, 2010
- A Hereditary Syndrome: "Dysplasia Oculodentodigitalis"Archives of Ophthalmology (1950), 1964
- The Holmes-Adie Syndrome in a Boy with Acute Juvenile Rheumatism and Bilateral SyndactylyArchives of Disease in Childhood, 1963