Abstract
The Vogt-Koyanagi-Harada syndrome (VKH) is a bilateral, severe granulomatous uveitis associated with serous retinal detachment, papillary edema and extra-ocular manifestations. Uveitis in children accounts for 5 to 10% of all uveitis cases; the VKH is rarely described in the children population. The diagnosis of this condition can be very challenging; especially if clinical diagnosis criteria are not being met at the onset of this affection. The visual prognosis is mostly good if the treatment is early started.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.