Cogan's Syndrome: 18 Cases and a Review of the LiteratureSubject Review Cogan's Syndrome: 18 Cases and a Review of the Literature RANDALL S. VOLLERTSEN, M.D., Division

Prolonged prodrome, systemic vasculitis, and deafness in Cogan’s syndrome S Van Doornum, G McColl, M Walter, I Jennens, P Bhathal, I P Wicks Abstract Cogan’s

Microsoft Word - Cogan's Syndrome brochure_B&W for website_PDF_11.29.2018 .docxCOGAN’S SYNDROME Page 1 of 5 Reproduction of this material requires written

R. Shihada et al • Vol 9 • January 200752 Cogan’s syndrome is a rare disorder, typi- cally defined by non-syphilitic interstitial keratitis associated with

NEUROLOGY2018963041 39..41Pearls & Oy-sters: Cogan syndrome A potentially grave disorder of audiovestibulopathy with many faces Sun-Uk Lee, MD, Ji-Soo Kim, MD, PhD, Joon

A shifty diagnosis: Cogan’s syndrome. A case report and review of the literatureCase report A shifty diagnosis: Cogan’s syndrome. A case report and review of

Cogan’s Syndrome with Cutaneous Findings: A Case Report and Review of Dermatologic Manifestations Khasha Touloei, DO,* Emily Tongdee, BS,** Brittany Smirnov, DO,***

PII: S0741-5214(99)70086-8Cogan’s syndrome is an autoimmune disease characterized by non-syphilitic interstitial keratitis and bilateral nerve deafness. The ophthalmologic

kalpABSTRACT: Cogan’s syndrome is a rare multi-systemic disease which is thought to be autoimmune in origin. It targets various organs, but all patients will suffer

162-1723-2-PB-2.pdfAbstract The autoimmune inner ear disease is a clinical syndrome with uncertain pathogenesis that is often associated to rapidly progres- sive hearing