Results 11 to 20 of about 137,343 (204)

Is it Vogt-Koyanagi-Harada syndrome?

open access: yesMedical Journal of Dr. D.Y. Patil University, 2015
Vogt-Koyanagi-Harada syndrome (VKH syndrome) is named after ophthalmologists Alfred Vogt from Switzerland and Yoshizo Koyanagi and Einosuke Harada from Japan.
Digambar Dashatwar   +2 more
doaj   +2 more sources

Enfermedad de Vogt Koyanagi Harada Bilateral: Reporte de un Caso [PDF]

open access: yesRevista Oftálmica
Objetivo: Reportar el  caso  de  una  paciente  diagnosticada con Enfermedad de Vogt Koyanagi Harada bilateral. Caso Clínico: Paciente femenina de 42 años, sin antecedentes médicos de importancia, quien consulta por visión borrosa en ojo derecho de 2 ...
Flor de María Chew Florián
doaj   +3 more sources

Síndrome de Vogt-Koyanagi-Harada [PDF]

open access: yesRevista de la Facultad de Ciencias Médicas de Córdoba, 2016
El síndrome de Vogt-Koyanagi-Harada es una enfermedad con hallazgos dermatológicos, neurológicos y auditivos, asociada con una panuveítis granulomatosa bilateral.
Juan Carlos Serna-Ojeda   +1 more
doaj   +4 more sources

Echographic findings in the late stages of Vogt-Koyanagi-Harada disease in mexican population

open access: yesRevista Brasileira de Oftalmologia, 2014
Purpose: To correlate clinical findings of Vogt-Koyanagi-Harada disease with standardized echography findings in a cross-sectional, descriptive and observational study.
Mariana Mayorquín-Ruiz   +4 more
doaj   +2 more sources

Vogt‐Koyanagi‐Harada disease‐like uveitis induced by nivolumab in metastatic renal cell carcinoma

open access: yesIJU Case Reports
Introduction Nivolumab can cause various immune‐related adverse events; it rarely induces Vogt‐Koyanagi‐Harada‐disease‐like uveitis. Vogt‐Koyanagi‐Harada‐disease is reported to be closely associated with human leukocyte antigen‐DR4.
Hitomi Imai   +9 more
doaj   +2 more sources

Síndrome de Vogt Koyanagi Harada [PDF]

open access: yesRevista Electrónica Dr. Zoilo E. Marinello Vidaurreta, 2014
Se presenta el caso de una paciente femenina de 28 años de edad, con síndrome de Vogt Koyanagi Harada (SVKH), con síntomas acompañantes de dolor ocular, cefalea y disminución de la visión en ambos ojos y con signos de hipoacusia e irritación meníngea. Se
Brunilda de los Angeles Aveleira Ortiz   +2 more
doaj   +2 more sources

Premature Ovarian Insufficiency in a Patient With Vogt-Koyanagi-Harada Syndrome: An Unusual Association-A Case Report. [PDF]

open access: yesCase Rep Med
Premature ovarian insufficiency (POI) is a clinical syndrome characterized by ovarian failure in women of reproductive age before the age of 40 years. Its main manifestations include menstrual cycle disturbances, such as oligomenorrhea or amenorrhea. The etiology of POI is highly heterogeneous, with a particular emphasis on genetic and immunological ...
Rocha RB   +7 more
europepmc   +2 more sources

A Case of Probable Vogt-Koyanagi-Harada Disease

open access: yesTürk Oftalmoloji Dergisi, 2012
The aim of this article is to present a rare form of Vogt-Koyanagi-Harada (VKH) disease. The complete and incomplete forms of VKH disease are more frequent than the probable form. A 58-year-old woman presented with bilateral painless blurred vision and headache. The patient’s visual acuity was 1/10 for both eyes. The patient had bilateral iridocyclitis,
Acar, Mutlu   +3 more
openaire   +6 more sources

Vogt Koyanagi Harada syndrome in a 15-year-old girl, steroids side effects and recurrences

open access: yesThe Turkish Journal of Pediatrics, 2021
Background. Vogt-Koyanagi-Harada Syndrome is rare in childhood and is usually seen between the 2nd and 5th decades. We present a 15-year-old girl with findings of incomplete Vogt-Koyanagi-Harada Syndrome. Case.
Gamze Yıldırım   +3 more
doaj   +1 more source

Image findings of Vogt-Koyanagi-Harada [PDF]

open access: yesArquivos de Neuro-Psiquiatria, 2013
Nivaldo Borges Nunes Junior   +3 more
doaj   +4 more sources

Home - About - Disclaimer - Privacy