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International Journal of Radiology and Diagnostic Imaging
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Peer Reviewed Journal

2025, Vol. 8, Issue 2, Part A

Wildervanck syndrome: A rare case of congenital hearing loss with cystic cochleovestibular malformation and cervical diastematomyelia
Author(s)
Nikhil R Mahajan, Anagha R Joshi and Chinmayee Chitnis
Abstract
Wildervanck syndrome is a rare genetic disorder, infrequently seen in the general population. The disorder affects ocular movements, hearing, and is associated with cervical spine anomalies. Along with these clinical manifestations, the affected population have a characteristic appearance on radiological imaging which aids in the diagnosis of this syndrome.
We present clinico-radiological findings in a 4-year-old child with a classical triad of Wildervanck syndrome associated with cervical diastematomyelia.
Pages: 04-07 | Views: 1136 | Downloads: 600


International Journal of Radiology and Diagnostic Imaging
How to cite this article:
Nikhil R Mahajan, Anagha R Joshi, Chinmayee Chitnis. Wildervanck syndrome: A rare case of congenital hearing loss with cystic cochleovestibular malformation and cervical diastematomyelia. Int J Radiol Diagn Imaging 2025;8(2):04-07. DOI: 10.33545/26644436.2025.v8.i2a.448
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