Vogt-koyanagi-harada syndrome
Joint Authors
al-Rifi, Mumin
Ayachit, Seemantini
Asal, Ahmad
al-Amir, Ahmad
Source
Issue
Vol. 37, Issue 1 (31 Mar. 2015)5 p.
Publisher
King Hamad University Hospital
Publication Date
2015-03-31
Country of Publication
Bahrain
No. of Pages
5
Main Subjects
Abstract EN
Vogt-Koyanagi-Harada (VKH) syndrome is a rare autoimmune multisystemic disease involving the melanocyte-containing organs; it is a diagnosis of exclusion.
The disease is progressive and has undesired complications.
We report the first case of VKH syndrome in the Kingdom of Bahrain.
The report aims to describe this rare syndrome with more emphasis on the ocular manifestations and management.
American Psychological Association (APA)
al-Amir, Ahmad& Asal, Ahmad& Ayachit, Seemantini& al-Rifi, Mumin. 2015. Vogt-koyanagi-harada syndrome. Bahrain Medical Bulletin،Vol. 37, no. 1.
https://search.emarefa.net/detail/BIM-603498
Modern Language Association (MLA)
Asal, Ahmad…[et al.]. Vogt-koyanagi-harada syndrome. Bahrain Medical Bulletin Vol. 37, no. 1 (Mar. 2015).
https://search.emarefa.net/detail/BIM-603498
American Medical Association (AMA)
al-Amir, Ahmad& Asal, Ahmad& Ayachit, Seemantini& al-Rifi, Mumin. Vogt-koyanagi-harada syndrome. Bahrain Medical Bulletin. 2015. Vol. 37, no. 1.
https://search.emarefa.net/detail/BIM-603498
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-603498
