This stage discuss about clinical lineaments, diagnosis, and management of Vogt-Koyanagi-Harada ailment. Vogt-Koyanagi-Harada disease (VKHD), initially defined as an uveomeningoencephalitic syndrome, is a systemic granulomatous autoimmune ailment that targets melanocyte-rich tissues, such as analysis, inner ear, meninges, skin and fiber. VKHD is difficult to diagnose cause its clinical performance is variable and multisystemic that often leads to late diagnosis and situation allowing the appearance and progress of the disease sequelae. We report a 35-year-traditional female presented to our hospital accompanying chief complaints of pain, redness, and liberal diminution of vision in two together eyes for 2 years. Early standard of comparison to tertiary centers should be values, as delay in initiation of treatment can bring about secondary complications in the way that serous retinal detachment, waterfall, glaucoma, choroidal.
Author(s) Details:
Pallavi Priyadarsani Sahu,
Department
of Ophthalmology, Kalinga Institute of Medical Sciences, Kalinga Institute of
Industrial Technology University, Bhubaneswar, Odisha, India.
Matuli
Das,
Department
of Ophthalmology, Kalinga Institute of Medical Sciences, Kalinga Institute of
Industrial Technology University, Bhubaneswar, Odisha, India.
Please see the link here: https://stm.bookpi.org/ACMMR-V11/article/view/12975
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