Syndrome de Waardenburg - Klein
- 1 July 1965
- journal article
- research article
- Published by Cambridge University Press (CUP) in Acta geneticae medicae et gemellologiae
- Vol. 14 (4) , 353-375
- https://doi.org/10.1017/s1120962300015079
Abstract
In a family with 528 members, in 7 generations, 162 (47% of the 347 examined patients) showed a Waardenburg syndrome. The frequencies of the different signs are as follows: lateral displacement of the canthi interni and lacrimal puncta: 76%; hyperplasia of the nose root: 54%; hyperplasia of the eyebrows: 52%; deafness: 9%; heterochromia of the iris: 9%; partial albinism: 6%.This publication has 2 references indexed in Scilit:
- WAARDENBURG'S SYNDROME IN FATHER AND DAUGHTERActa Ophthalmologica, 1962
- Deafness as Part of an Hereditary SyndromeThe Journal of Laryngology & Otology, 1959