Assoc. Prof. M.D. Ahmet Yeşilyurt Reviews
Patient Experience
At 72, my unexplained muscle weakness baffled local doctors for years. Dr. Yeşilyurt ordered a specialized genetic panel that revealed a rare mitochondrial DNA deletion. His team created a personalized supplement protocol that restored my mobility within months. I can now garden again, thanks to his detective work in my very genes.
Our newborn son failed his hearing screening, but Dr. Yeşilyurt looked beyond the obvious. Genetic testing identified Pendred syndrome, allowing him to coordinate with ENT specialists for early intervention. He explained the inheritance pattern with such clarity that our entire family underwent counseling. We feel prepared, not scared.
As a 28-year-old athlete, my sudden cardiac episode was terrifying. Dr. Yeşilyurt diagnosed Long QT syndrome type 2 through genetic analysis. He didn't just prescribe medication; he designed a safe exercise regimen and connected me with a community of patients with the same condition. He turned a life-limiting diagnosis into a manageable reality.
Our daughter had mysterious seizures that no medication controlled. Dr. Yeşilyurt identified a KCNQ2 gene mutation through advanced exome sequencing. His targeted treatment plan stopped the seizures within weeks. He gave us back our smiling, developing child when we had lost all hope.
