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Ocular Findings in a Patient with Scheie Syndrome

Authors
Kim, Min SeongCho, In Hwan
Issue Date
Jun-2020
Publisher
대한안과학회
Keywords
Corneal clouding; Mucopolysaccharidosis; Retinal degeneration; Scheie syndrome
Citation
대한안과학회지, v.61, no.6, pp 685 - 689
Pages
5
Journal Title
대한안과학회지
Volume
61
Number
6
Start Page
685
End Page
689
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/2798
DOI
10.3341/jkos.2020.61.6.685
ISSN
0378-6471
2092-9374
Abstract
Purpose: To report ocular findings in a patient with Scheie syndrome. Case summary: A 28-year-old male who was diagnosed with Scheie syndrome ten years ago visited our ophthalmology clinic. The man was diagnosed with Scheie syndrome based on normal intelligence, a coarse face, cardiac valve problems, and reduced alpha-L-iduronidase, heparan sulfate and dermatan sulfate levels on urinalysis. An ophthalmic examination showed that the best-corrected visual acuities were 0.25 and 0.2, while the intraocular pressures were 11 and 12 mmHg, in the right and left eyes, respectively. An anterior segment examination was normal except for corneal clouding (grade II). Fundus examination revealed bony spicule pigmentation in the peripheral retina and vessel attenuation in both eyes. Parafoveal photoreceptor loss was revealed by optical coherence tomography. In addition, scotopic and photopic electroretinographic responses were decreased, and the visual field decreased in accordance with the photoreceptor cell loss. Conclusions: Clinicians should consider a diagnosis of Scheie syndrome when examining a patient with characteristic ocular findings and general symptoms.
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