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Revista Cubana de Oftalmología

ISSN 1561-3070 (Electronic)
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2015, Number 1

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Rev Cub Oftal 2015; 28 (1)

Vogt-Koyanagi-Harada disease and visual rehabilitation

Quintero BM, Vilches LDC, Bueno AY, Rodríguez MS, Perea RCA, Paz LM
Full text How to cite this article

Language: Spanish
References: 18
Page: 146-151
PDF size: 83.29 Kb.


Key words:

Vogt-Koyanagi-Harada disease, optical aid, non-optical aid, low vision, legally blind, visual rehabilitation.

ABSTRACT

Vogt-Koyanagi-Harada (VKH) is a rare, multisystemic, allegedly autoimmune disease of unknown etiology. It is characterized by chronic bilateral granulomatous and diffuse panuveitis, accompanied by tegumentary, neurological and hearing impairments that often affect the non-Caucasians and usually women. It usually occurs in the 20-25 years age group and its incidence varies with the geographic location. It is estimated that 25% of the patients with this disease are legally blind, the other 25% may have low vision and 50% present with visual acuity over 20/50. There is a 50 years-old patient with a history of Vogt - Koyanagi - Harada disease for 8 years. He had been treated with systemic steroid anti-inflammatory drugs and immunosuppressive therapy as well as supporting therapy with topical and cycloplegic steroid anti-inflammatories. The patient had gone to the low vision service looking for rehabilitation. He was performed a complete eye examination, supplementary studies and he was finally rehabilitated through the use of optical and non-optical aids in order to maximize his remaining vision.


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Rev Cub Oftal. 2015;28