PROBABLE VOGT-KOYANAGI-HARADA DISEASE: A CASE REPORT
Vogt-Koyanagi-Harada(VKH)diseaseisabilateralgranulomatouspanuveitis affecting young adults, withor without systemic manifestations. The prognosis of VKH disease is generally favorable, however the development of complicationscanleadto blindnessanddeafness.(1) In this case, we report a 22-year-old ma...
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| Veröffentlicht in: | International journal of advanced research (Indore) 2023-02, Vol.11 (2), p.1257-1261 |
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| container_title | International journal of advanced research (Indore) |
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| creator | M., Elakhdari Y., Akannour C., Bardi K., Mrad S., Hassina L., Serghini A., El Hassan A., Berraho |
| description | Vogt-Koyanagi-Harada(VKH)diseaseisabilateralgranulomatouspanuveitis affecting young adults, withor without systemic manifestations. The prognosis of VKH disease is generally favorable, however the development of complicationscanleadto blindnessanddeafness.(1) In this case, we report a 22-year-old man who developed probable Vogt–Koyanagi–Haradadisease without any systemic symptoms, but with several risk factors for poor visual prognosisbeforetreatment,andwhowassuccessfullytreatedwithintensivecorticosteroidtherapy. Our aim is to describe a clinical case with bilateral serous retinal detachment that presumed asprobableVKHdisease. |
| doi_str_mv | 10.21474/IJAR01/16375 |
| format | Article |
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| title | PROBABLE VOGT-KOYANAGI-HARADA DISEASE: A CASE REPORT |
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