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Wilson Disease Combined with Keratoconus: A Case Report
Adem Tellioglu1, Derya Ozkan1, Burcin Kepez Yildiz1
1Department of Ophthalmology, University of Health Sciences Beyoglu Eye Training and Research Hospital, İstanbul, Türkiye.
This case report details a rare co-occurrence of Wilson disease (WD) and keratoconus (KC) in a 30-year-old male. The patient presented with vision loss, revealing copper deposits and corneal changes consistent with KC.
Area of Science:
- Ophthalmology
- Genetics
- Neurology
Background:
- Wilson disease (WD) is a rare autosomal recessive disorder of copper metabolism.
- Keratoconus (KC) is a progressive thinning and ectasia of the cornea.
- The co-occurrence of WD and KC is exceptionally rare, with limited reported cases.
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