Autor: |
Al Amer, Ahmed, Asal, Ahmed, Ayachit, Seemantini, Al Reefy, Moemen |
Předmět: |
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Zdroj: |
Bahrain Medical Bulletin; Mar2015, Vol. 37 Issue 1, p113-117, 5p |
Abstrakt: |
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. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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