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Information Journal Paper

Title

COGAN'S SYNDROME: A CASE REPORT

Pages

  222-225

Abstract

 Cogan's syndrome (CS) is an immune-mediated disease characterized by ocular in-flammation and audiovestibular dysfunction with or without VASCULITIS or other systemic manifestations (1). Audiovestibular disease that is difficult to treat can lead to the loss of hearing (2). By a timely recognition and initiation of glucocorticoid therapy at the onset of the disease, poor outcomes, especially complete hearing loss, could sometimes be prevented (2). Certain patients may require long-term corticosteroid therapy because of recurrent hearing loss during attempts to taper the prednisone dose (3). We report COGAN’S SYNDROME in a 14 year-old-girl with marked deterioration of hearing power fol-lowing tapering of corticosteroid therapy.

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    Cite

    APA: Copy

    AL RASHIDI, ABDULRAHMAN, MAREY, ATEF ALI, & HEGAZI, MOHAMED OSAMA. (2008). COGAN'S SYNDROME: A CASE REPORT. IRANIAN JOURNAL OF IMMUNOLOGY (IJI), 5(4), 222-225. SID. https://sid.ir/paper/296829/en

    Vancouver: Copy

    AL RASHIDI ABDULRAHMAN, MAREY ATEF ALI, HEGAZI MOHAMED OSAMA. COGAN'S SYNDROME: A CASE REPORT. IRANIAN JOURNAL OF IMMUNOLOGY (IJI)[Internet]. 2008;5(4):222-225. Available from: https://sid.ir/paper/296829/en

    IEEE: Copy

    ABDULRAHMAN AL RASHIDI, ATEF ALI MAREY, and MOHAMED OSAMA HEGAZI, “COGAN'S SYNDROME: A CASE REPORT,” IRANIAN JOURNAL OF IMMUNOLOGY (IJI), vol. 5, no. 4, pp. 222–225, 2008, [Online]. Available: https://sid.ir/paper/296829/en

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