---
abstract: 'The Vogt-Koyanagi-Harada (VKH) syndrome is a rare systemic disorder of uveitis, dysacousia, vitiligo, premature graying of the hair, eyebrows and eyelashes, and meningoencephalitis. Although frequently unrecognised,VKH may affect children.  We report a case of a 10 year old girl who presented with headache and dimness of vision and was diagnosed as papillitis on the basis of bilateral disc edema. However over the course of time developed skin changes (poliosis, vitiligo over lower back) and depigmented patches in inferior fundus  suggesting  diagnosis of VKH disease. Thus the diagnosis is difficult in the absence of extraocular manifestations. In such cases the diagnosis is based on clinical evolution of the disease.'
altloc:
  - http://www.ojhas.org/issue38/2011-2-24.htm
chapter: ~
commentary: ~
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conference: ~
confloc: ~
contact_email: ~
creators_id:
  - aaliarasool_s@yahoo.com
  - ~
  - ~
creators_name:
  - family: Sufi
    given: AR
    honourific: ''
    lineage: ''
  - family: Zargar
    given: S
    honourific: ''
    lineage: ''
  - family: Singh
    given: T
    honourific: ''
    lineage: ''
date: 2011-07-30
date_type: published
datestamp: 2012-11-09 17:37:20
department: ~
dir: disk0/00/00/79/86
edit_lock_since: ~
edit_lock_until: 0
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editors_id:
  - BS Kakkilaya
editors_name:
  - family: Kakkilaya
    given: Srinivas
    honourific: Dr
    lineage: ~
eprint_status: archive
eprintid: 7986
fileinfo: application/pdf;http://cogprints.org/7986/1/2011%2D2%2D24.pdf
full_text_status: public
importid: ~
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isbn: ~
ispublished: pub
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item_issues_comment: []
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item_issues_resolved_by: []
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keywords: Vogt-Koyanagi-Harada Syndrome; Poliosis; Vitiligo; Uveitis.
lastmod: 2012-11-09 17:37:20
latitude: ~
longitude: ~
metadata_visibility: show
note: ~
number: 2
pagerange: ~
pubdom: TRUE
publication: Online Journal of Health and Allied Sciences
publisher: BS Kakkilaya
refereed: TRUE
referencetext: "1.\tMoorthy RS, Inomata H, Rao NA. Vogt-Koyanagi-Harada syndrome. Surv Ophthalmol 1995;39:265-292.\r\n2.\tVogt A. Fruhzeitiges Ergrauen der Zilien und Bemerkungen uber den sogenannten plotzlichen Eintritt dieser Veranderung. Klin Monatsbl Augenheilk 1906;44:228-242.\r\n3.\tKoyanagi Y. Dysakusis, Alopecia und Poliosis bei schwerer Uveitis nicht trauma-tischen Ursprungs. Klin Monatsbl Augenheilk 1929;82:194-211.\r\n4.\tHarada E. On the acute diffuse choroiditis. Acta Soc Ophthalmol Jpn 1926;30:356-378.\r\n5.\tSuguira S. Vogt-Koyanagi-Harada disease. Jpn J Ophthalmol 1978;22:9-35.\r\n6.\tInomata H. Vogt-Koyanagi-Harada Disease. In: Yanoff  M, Duker JS, editors. Ophthalmology. 2nd  ed. Missouri: Mosby; 2004. pp. 1196-1198.\r\n7.\tRussel WR, Holland GN, Rao NA, Tabarra KF, Ohno S, Arellanes-Garcia L, et al. Revised diagnostic criteria for Vogt-Koyanagi-Harada disease: report of an International Committee on Nomenclature. Am J Ophthalmol 2001;131:647-652.\r\n8.\tRathinam SR, Vijayalakshmi P, Namperumalsamy P, Nozik RA, Cunningham ET. Vogt-Koyanagi-Harada syndrome in children. Ocular Immunology & Inflammation1998;6(3):155-161.\r\n9.\tSawhney R, Jain R, Kumar S, Pannu BKS, Sood S. Glucose intolerance and Vogt-Koyanagi-Harada Syndrome. Asian Journal of Ophthalmol 2002;4:8-10."
relation_type: []
relation_uri: []
reportno: ~
rev_number: 9
series: ~
source: ~
status_changed: 2012-01-26 07:12:16
subjects:
  - OJHAS
succeeds: ~
suggestions: ~
sword_depositor: ~
sword_slug: ~
thesistype: ~
title: Vogt-Koyanagi-Harada Syndrome in a 10 Years Old Child
type: journale
userid: 4338
volume: 10
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