Results 161 to 170 of about 137,343 (204)
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Archives of Otolaryngology - Head and Neck Surgery, 1967
THE VOGT-KOYANAGI-HARADA (VKH) syndrome is a relatively rare multisystem disease. This syndrome has been frequently reported by ophthalmologists; however, there has been a noticeable absence in the otolaryngologic literature. The most consistent finding is uveitis. It may also include alopecia, poliosis, vitiligo, and dysacousia. Through the years the
R L, Seals, E N, Rise
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THE VOGT-KOYANAGI-HARADA (VKH) syndrome is a relatively rare multisystem disease. This syndrome has been frequently reported by ophthalmologists; however, there has been a noticeable absence in the otolaryngologic literature. The most consistent finding is uveitis. It may also include alopecia, poliosis, vitiligo, and dysacousia. Through the years the
R L, Seals, E N, Rise
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American Journal of Ophthalmology, 1977
We studied 51 patients who developed Vogt-Koyanagi-Harada (V-K-H) syndrome after corticosteroid therapy. The final visual acuity was better than 6/15 (20/50) in 50%, and less than 6/60 (20/200) in 25% of the patients. The severity and extraocular manifestations of this disease also appeared to be less than observed in patients before the clinical use ...
S, Ohno +3 more
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We studied 51 patients who developed Vogt-Koyanagi-Harada (V-K-H) syndrome after corticosteroid therapy. The final visual acuity was better than 6/15 (20/50) in 50%, and less than 6/60 (20/200) in 25% of the patients. The severity and extraocular manifestations of this disease also appeared to be less than observed in patients before the clinical use ...
S, Ohno +3 more
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Current Opinion in Ophthalmology, 2000
Vogt-Koyanagi-Harada (VKH) disease affects primarily persons who are Asian, Latino, Native American, or Asian Indian. Women appear to be affected more commonly than men, and VKH disease may occur at all ages, including childhood. Experimental data continue to support an autoimmune etiology for VKH disease, directed most probably against an antigenic ...
R W, Read, N A, Rao, E T, Cunningham
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Vogt-Koyanagi-Harada (VKH) disease affects primarily persons who are Asian, Latino, Native American, or Asian Indian. Women appear to be affected more commonly than men, and VKH disease may occur at all ages, including childhood. Experimental data continue to support an autoimmune etiology for VKH disease, directed most probably against an antigenic ...
R W, Read, N A, Rao, E T, Cunningham
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Ocular Immunology and Inflammation, 2014
Vogt-Koyanagi-Harada (VKH) disease is an autoimmune disorder characterized in its complete form by the occurrence of bilateral uveitis accompanied by dermatologic as well as neurologic or auditory ...
Emmett T, Cunningham +4 more
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Vogt-Koyanagi-Harada (VKH) disease is an autoimmune disorder characterized in its complete form by the occurrence of bilateral uveitis accompanied by dermatologic as well as neurologic or auditory ...
Emmett T, Cunningham +4 more
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Vogt-Koyanagi-Harada disease in Spain
European Journal of Ophthalmology, 2021Purpose: To describe the clinical and epidemiological characteristics of patients with Vogt-Koyanagi-Harada (VKH) disease in Spain. Methods: This was a retrospective multicenter analysis of data from VKH patients followed for at least ...
Pedro Arriola-Villalobos +22 more
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Acta Ophthalmologica, 1993
Abstract. The case history is presented of a 40‐year‐old White woman with the Vogt‐Koyanagi‐Harada syndrome, who was successfully treated with a combination of low‐dose prednisolone and cyclosporine A. Cellular and humoral hypersensitivity to uveal and retinal antigens were demonstrated in the patient.
H, Hammer, M, Janáky, I, Süveges
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Abstract. The case history is presented of a 40‐year‐old White woman with the Vogt‐Koyanagi‐Harada syndrome, who was successfully treated with a combination of low‐dose prednisolone and cyclosporine A. Cellular and humoral hypersensitivity to uveal and retinal antigens were demonstrated in the patient.
H, Hammer, M, Janáky, I, Süveges
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Ophthalmology Clinics of North America, 2002
Vogt-Koyanagi-Harada disease is a chronic, granulomatous systemic autoimmune disease with manifestations in the ocular, central nervous, auditory, and integumentary systems. The target of attack seems to be antigens associated with melanocytes. Patients are usually of Asian, Middle Eastern, Asian Indian, Native American, or Hispanic ethnicity, and ...
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Vogt-Koyanagi-Harada disease is a chronic, granulomatous systemic autoimmune disease with manifestations in the ocular, central nervous, auditory, and integumentary systems. The target of attack seems to be antigens associated with melanocytes. Patients are usually of Asian, Middle Eastern, Asian Indian, Native American, or Hispanic ethnicity, and ...
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Vogt-Koyanagi-Harada syndrome in children
Ocular Immunology and Inflammation, 1998To describe the clinical presentation and natural history of Vogt-Koyanagi-Harada (VKH) syndrome in children, an often unrecognized cause of pediatric uveitis.We performed a clinic-based cross-sectional survey and retrospective review of pediatric patients with VHK seen in the uveitis clinic at the Aravind Eye Hospital, Madurai, India, between January ...
S R, Rathinam +4 more
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Deafness in Vogt–Koyanagi–Harada syndrome
The Journal of Laryngology & Otology, 2006Sudden onset sensorineural hearing loss is a well recognized entity frequently encountered in otolaryngological practice. However, the combination of such deafness as part of a wider systemic disorder is fortunately rare. Almost 100 years after the syndrome was classified, we describe a case of Vogt–Koyanagi–Harada syndrome occurring unusually in a ...
A, Sil, P, Chatrath, D J, Gatland
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Acta Ophthalmologica, 1986
Abstract A 32‐year‐old Norwegian woman was admitted to the University department of Ophthalmology with marked subretinal oedema in both eyes and slight flare in the anterior chambers. Vision was reduced to counting fingers at 1 m o.d. and 6/24 o.s. Lumbal puncture revealed pleocytosis, and antimyelin antibodies were found in the serum confirming and ...
T H, Iversen, T, Sverrisson
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Abstract A 32‐year‐old Norwegian woman was admitted to the University department of Ophthalmology with marked subretinal oedema in both eyes and slight flare in the anterior chambers. Vision was reduced to counting fingers at 1 m o.d. and 6/24 o.s. Lumbal puncture revealed pleocytosis, and antimyelin antibodies were found in the serum confirming and ...
T H, Iversen, T, Sverrisson
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