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Current Opinion in Ophthalmology, 2015
The purpose of this article is to review the current literature on Vogt-Koyanagi-Harada (VKH) disease, including current treatment options and new research directions.Recent publications on VKH disease show an increased focus on the immunogenetics and immune pathways associated with the development of VKH disease.
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The purpose of this article is to review the current literature on Vogt-Koyanagi-Harada (VKH) disease, including current treatment options and new research directions.Recent publications on VKH disease show an increased focus on the immunogenetics and immune pathways associated with the development of VKH disease.
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Archives of Dermatology, 1963
The clinical findings in the Vogt-Koyanagi-Harada syndrome are reviewed and a case reported emphasizing the cutaneous changes. The syndrome consists of symptoms of meningeal irritation, nontraumatic uveitis, poliosis, vitiligo, alopecia, and dysacousia.
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The clinical findings in the Vogt-Koyanagi-Harada syndrome are reviewed and a case reported emphasizing the cutaneous changes. The syndrome consists of symptoms of meningeal irritation, nontraumatic uveitis, poliosis, vitiligo, alopecia, and dysacousia.
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The Vogt - Koyanagi - Harada Syndrome in Children
Journal of Pediatric Ophthalmology & Strabismus, 1977Two cases of the Vogt--Koyanagi--Harada syndrome in children, a very rare disorder in this age group, are reported; one patient had the chronic diffuse type, and the other had neurologic symptoms and exudative retinal detachments. Various theories of causation of the syndrome have been proposed, including viral infection, sympathetic ophthalmia, and ...
S W, Weber, J J, Kazdan
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Medicina Clínica (English Edition), 2016
Vogt–Koyanagi–Harada disease is a bilateral granulomatous panuveitis, generally symmetrical, associated to extraocular manifestations such as poliosis, vitiligo, alopecia, central nervous system, and auditory signs. It is considered an autoimmune disease, mediated by T cells, against melanocytes of uveal tract, skin, central nervous system, and inner ...
Jorge Ortiz Balbuena +3 more
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Vogt–Koyanagi–Harada disease is a bilateral granulomatous panuveitis, generally symmetrical, associated to extraocular manifestations such as poliosis, vitiligo, alopecia, central nervous system, and auditory signs. It is considered an autoimmune disease, mediated by T cells, against melanocytes of uveal tract, skin, central nervous system, and inner ...
Jorge Ortiz Balbuena +3 more
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Pathology of Vogt–Koyanagi–Harada disease
International Ophthalmology, 2007Typical histopathologic features of Vogt-Koyanagi-Harada disease (VKH) include granulomatous panuveitis with preservation of the choriocapillaris and exudative retinal detachment. In the chronic stage of the disease, however, histologic changes consist of nongranulomatous uveitis followed, in the chronic recurrent stage, by granulomatous uveitis and ...
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A.M.A. Archives of Ophthalmology, 1957
A prodromal meningismal episode, followed by nontraumatic bilateral uveitis, followed later by vitiligo, alopecia, dysacousia, and poliosis are the essential features of the Vogt-Koyanagi syndrome. 1 If retinal detachment is detected in the course of the illness, the diagnosis has been made.of Harada's disease.
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A prodromal meningismal episode, followed by nontraumatic bilateral uveitis, followed later by vitiligo, alopecia, dysacousia, and poliosis are the essential features of the Vogt-Koyanagi syndrome. 1 If retinal detachment is detected in the course of the illness, the diagnosis has been made.of Harada's disease.
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Vogt‐Koyanagi‐Harada Disease in an Adolescent Boy
Pediatric Dermatology, 2013AbstractVogt‐Koyanagi‐Harada (VKH) disease is a rare multiorgan disorder that affects the melanocytes of the eyes, skin, inner ear, and meninges. It is more common in women and in patients 30 to 50 years of age; it is rarely seen in children. We report a 14‐year‐old boy who meets the criteria for complete VKH disease.
Bilgic, Ozlem +2 more
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Uveomeningoencephalitic Syndrome (Vogt-Koyanagi-Harada)
Archives of Neurology, 1965UVEOMENINGOENCEPHALITIC syndrome (Vogt-Koyanagi-Haranda [VKH]) is an unusual syndrome with important neurological complications and has not, to my knowledge, been discussed in English in the neurological literature. VKH is a multisystem disorder and includes idiopathic uveitis, dysacousia, leukodermia, alopecia, canities (whitened hair), poliosis ...
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Vitiligo and the Vogt-Koyanagi-Harada Syndrome
Dermatologic Clinics, 1988Vitiligo is a common acquired systemic disease that can be associated with several different autoimmune disorders. Besides the psychologically upsetting depigmentation of the skin that it causes, it can be associated with ocular abnormalities. There are three different theories regarding the etiology of vitiligo, none of which is entirely satisfactory.
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Medicina Clínica (English Edition), 2015
Aldo René, Hurtarte Sandoval +3 more
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Aldo René, Hurtarte Sandoval +3 more
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