Abstract
A 15-year-old female was found to have the typical features of Wildervanck's syndrome, including Klippel-Feil anomaly, abducens paralysis, retraction of the bulbi, and deafness. In addition, she had bilateral lens subluxation and facial paralysis, neither of which have been reported in patients with Wildervanck's syndrome.
Full text
PDF
Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Kirkham T. H. Cervico-oculo-acusticus syndrome with pseudopapilloedema. Arch Dis Child. 1969 Aug;44(236):504–508. doi: 10.1136/adc.44.236.504. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Say B., Balci S., Israel R., Yalaz K., Tinaztepe B., Erbengi A., Sümer N. Cervico-ocula-acusticus syndrome of Wildervanck. Case report. Turk J Pediatr. 1973 Jul;15(3):157–163. [PubMed] [Google Scholar]
- WILDERVANCK L. S. [A cervico-oculo-acoustic nerve syndrome]. Ned Tijdschr Geneeskd. 1960 Dec 24;104:2600–2605. [PubMed] [Google Scholar]
- Wildervanck L. S., Hoeksema P. E., Penning L. Radiological examination of the inner ear of deaf-mutes presenting the cervico-oculo-acusticus syndrome. Acta Otolaryngol. 1966 May;61(5):445–453. doi: 10.3109/00016486609127082. [DOI] [PubMed] [Google Scholar]