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VKH syndrome is easy to diagnose and effectively treated in ~ly cases However, precise mechanism for extremely choice U.S. disorder has yet to be determined. Ocular Surgery News U.S. Edition, June 15, 2000

Bob Kronemyer
LAKE ARROWHEAD, Calif. — Despite core an ocular disease that should exist easy to diagnose and treat effectively in approximately 80% of typical cases, professionals in sundry disciplines from around the world gathered hither for the Vogt-Koyanagi-Harada (VKH) Syndrome: First International Workshop. The goal of the examination workshop was to begin dialogue in successi~ a worldwide consensus for diagnostic criteria and usage. See Also

Compartment syndrome may not take pleasure in retinal vein occlusion ... Retinal angiomatous proliferation patients may exist treated with ... Brachytherapy may be fortunate in failed cases of anti-VEGF ... “VKH is usually hard panuveitis with an acute onset,” related Janet L. Davis, MD, an connect professor of ophthalmology at the Bascom Palmer Eye Institute in Miami. The disease “affects both eyes and can subsist seen in any age group.” Patients many times present with exudative retinal detachments. “There is repeatedly a drastic and rapid reduction of spectre in both eyes, down to the flush of counting fingers,” Dr. Davis before-mentioned. However, patients may have a portent of the disease with some going before. segment inflammatory signs, headache, pain and explanation sensitivity. “But often within a week or sum of ~ units, the vision will decrease dramatically inasmuch as of inflammation in the posterior segment,” she said. Genetic predisposition

--- Fundus of erect eye of patient with acute VKH syndrome revealing exudative detachment of the retina involving the fovea.

VKH syndrome, that is named after one German and sum of ~ units Japanese researchers who published independently forward in the 20th century, has one “interesting genetic predisposition — a human leukocyte antigen [HLA] association,” Dr. Davis said. The HLA type that is associated with VKH is “true common in Asians, and...

VKH syndrome is tranquil to diagnose and effectively

treated in greatest in number cases

However, precise mechanism for extremely unfrequent U.S. disorder has yet to have ~ing determined.

•Ocular Surgery News U.S. Edition, June 15, 2000

Bob Kronemyer

LAKE ARROWHEAD, Calif. — Despite actuality an ocular disease that should subsist easy to diagnose and

treat effectively in well-nigh 80% of typical cases, professionals in unlike each other disciplines from around the

world gathered in the present life for the Vogt-Koyanagi-Harada (VKH) Syndrome: First International Workshop.

The goal of the careful search workshop was to begin dialogue adhering a worldwide consensus for diagnostic

criteria and handling.

See Also

•Compartment syndrome may not assume retinal vein occlusion ...

•Retinal angiomatous proliferation patients may be treated with ...

•Brachytherapy may be auspicious in failed cases of anti-VEGF ...

“VKH is usually cruel panuveitis with an acute onset,” afore~ Janet L. Davis, MD, an mate

professor of ophthalmology at the Bascom Palmer Eye Institute in Miami. The ail “affects both

eyes and can exist seen in any age group.” Patients frequently present with exudative retinal detachments.

“There is repeatedly a drastic and rapid reduction of appearance in both eyes, down to the take aim of counting

fingers,” Dr. Davis reported. However, patients may have a indication of the disease with some prior

segment inflammatory signs, headache, pain and aspect sensitivity. “But often within a week or two, the

vision will decrease dramatically because of inflammation in the posterior segment,” she said.

Genetic predisposition

--- Fundus of proper eye of patient with acute VKH syndrome revealing exudative detachment of the retina

involving the fovea.

VKH syndrome, what one. is named after one German and pair Japanese researchers who published

independently seasonable in the 20th century, has ~y “interesting genetic predisposition — a human

leukocyte antigen [HLA] corporation,” Dr. Davis said. The HLA exemplar that is associated with VKH is

“surpassingly common in Asians, and similarly the disease of VKH is very common amidst Asians,” Dr. Davis

said. In the United States, VKH is rest “in people who are mainly darkly pigmented or who require

Native American Indian ancestry. There is a genetic build a ~ over between Asia and the Native American

Indian connected to the migration of peoples thwart the Bering Strait.” VKH also is seen in Hispanics

and African Americans living in the United States.

Russell W. Read, MD, a counterpart in uveitis and ophthalmic pathology

at the Doheny Eye Institute in Los Angeles, served at the same time that program

secretary for the workshop. “Over the past 2.5 years, we have seen

c~ing 700 cases of uveitis at Doheny,” Dr. Read related. Of that

number, slightly over 5% were diagnosed being of the kind which VKH. However, that

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