Cogan’s Syndrome

Cogan’s Syndrome is a rare autoimmune vasculitis characterised by recurrent ocular inflammation—most often interstitial keratitis—and vestibulo-auditory dysfunction resembling Ménière’s disease. It may extend systemically, affecting the aorta and medium vessels, leading to serious cardiovascular complications. Diagnosis is clinical, supported by ophthalmologic, audiometric, and imaging evaluations. Beyond corticosteroids and immunosuppressants, a regenerative approach integrates AASI, PSC, GcMAF Forte, and Thymus Therapy with MO/NOP Thymus and MO/NOP STF to rebalance immunity, protect neurovascular structures, and preserve sensory function.