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