Usher Syndrome

  • Ana Fakin
  • Damjan Glavač
  • Marko Hawlina

Abstract

Usher syndrome is an autosomal recessive disease with prevalence of 3–6/100.000 and is the most common syndrome that affects vision and hearing. Three subtypes are distinguished on the basis of different degree of hearing loss. All patients develop retinitis pigmentosa with night vision difficulties and constriction of visual field, and ultimately a decline in visual acuity and color vision. Future holds promise for gene therapy. We present a patient with typical clinical picture of Usher syndrome, who started noticing night vision problems at age 13. At age 25 he was operated on for posterior cortical cataracts. At age 34 he has only 5–10° of visual field remaining with 1.0 visual acuity in both eyes. Fundus autofluorescence imaging revealed a typical hyperautofluorescent ring on the border between normal and affected retina.

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Published
2012-06-15
How to Cite
1.
Fakin A, Glavač D, Hawlina M. Usher Syndrome. ZdravVestn [Internet]. 15Jun.2012 [cited 22Sep.2019];82. Available from: https://vestnik.szd.si/index.php/ZdravVest/article/view/940
Section
Review