Vogt–Koyanagi–Harada Syndrome (VKHS): First Two Cases Reported in Pediatric Age Group in Oman

Author:

Al Hashmi Samiya1ORCID,Al Habsi Nasra2,Al Abrawi Safiya1ORCID

Affiliation:

1. Department of Child Health, Pediatric Rheumatology Unit, Royal Hospital, Muscat, Oman

2. Department of Ophthalmology, Ophthalmology Unit, Al Nahdah Hospital, Muscat, Oman

Abstract

The Vogt–Koyanagi–Harada syndrome (VKHS) is a unique form of granulomatous autoimmune disease that mostly impacts the pigmented tissues of the body. The main feature is bilateral granulomatous panuveitis, which is detected on ophthalmologic examination, along with additional systemic signs such as vitiligo, white hair, neurological involvement, or hearing loss. This study aims to report two cases of Vogt–Koyanagi–Harada syndrome presented in the children age group, which is unusual and very rare, to improve recognition of this disease to avoid complications and delay referral.

Publisher

Hindawi Limited

Subject

General Medicine

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