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Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
Corneal depositions in tyrosinaemia type I during treatment with Nitisinone
  1. Robert P L Wisse1,
  2. Dienke Wittebol-Post1,
  3. Gepke Visser2,
  4. Allegonda van der Lelij1
  1. 1Department of Ophthalmology, UMC Utrecht, Utrecht, The Netherlands
  2. 2Department of Metabolic Diseases, UMC Utrecht, Utrecht, The Netherlands
  1. Correspondence to Dr Robert PL Wisse, r.p.l.wisse{at}umcutrecht.nl

Summary

We present a 17-year-old boy, diagnosed with tyrosinaemia type I at an age of 7 months, with new complaints of severe intermittent photophobia and burning eyes. His tyrosinaemia type I is treated with nitisinone and a protein-restricted diet. Dietary compliance is low since he entered puberty. His ocular complaints are attributable to subepithelial corneal deposits, resembling the common corneal phenotype of tyrosinaemia type II. Serum tyrosine levels were markedly elevated. Tyrosinaemia is a metabolic disease of tyrosine metabolism, subdivided into two types. Corneal deposits and photophobia are cardinal features of untreated tyrosinaemia type II, but not of type I. Novel treatment strategies (with nitisinone) for type I tyrosinaemia lead to a phenotype comparable with type II, including these corneal deposits. At follow-up visits his ocular complaints unfortunately remained unchanged, though he states his dietary compliance improved through the years.

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