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JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2018; 28 (4): 325-326
in English | IMEMR | ID: emr-194858
ABSTRACT
Vogt-Koyanagi-Harada syndrome is a rare disease that occurs commonly in pigmented individuals of Asian origin. A 25-year female presented in medical outpatient department [OPD] of Al-Khidmat Teaching Hospital, Mansoora, Lahore with headache and neck stiffness. She was referred to eye OPD for the complaint of decreased vision. On examination, there was 6/24 vision, sluggish pupillary reaction and disc hyperemia in both eyes. She was treated as a case of optic neuritis. Few days later, she developed bilateral panuveitis, shallow exudative detachments and alopecia. Clinical picture with normal magnetic resonance imaging [MRI] and laboratory tests helped us in reaching the diagnosis of Vogt-KoyanagiHarada syndrome
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Index: IMEMR (Eastern Mediterranean) Language: English Journal: J. Coll. Physicians Surg. Pak. Year: 2018

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Index: IMEMR (Eastern Mediterranean) Language: English Journal: J. Coll. Physicians Surg. Pak. Year: 2018