JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2018; 28 (4): 325-326
en Inglés
| 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
Buscar en Google
Índice:
IMEMR (Mediterraneo Oriental)
Idioma:
Inglés
Revista:
J. Coll. Physicians Surg. Pak.
Año:
2018
Similares
MEDLINE
...
LILACS
LIS