While Coganās syndrome pairs interstitial keratitis with severe vestibulocochlear failure, Vogt-Koyanagi-Harada (VKH) syndrome is a systemic autoimmune disorder targeting melanocyte-rich tissues. VKH presents with bilateral panuveitis, meningismus, sensorineural hearing loss, dysacousia, and cutaneous depigmentation (vitiligo, poliosis), requiring aggressive systemic immunosuppression. How do you coordinate multisystem evaluations when autoimmune inner ear disease is suspected?