M.D. Murat Çağlar Reviews

Our 14-year-old competitive gymnast, Elif, developed a mysterious fatigue syndrome that baffled local doctors. Dr. Çağlar didn't just run tests—he spent an afternoon watching her training videos, noticing subtle coordination changes others missed. He diagnosed a rare metabolic disorder triggered by growth spurts. His customized nutrition and training modification plan didn't just restore her health—she qualified for nationals six months later.

When 3-day-old Arda stopped breathing during a routine checkup, Dr. Çağlar performed an emergency tracheal intubation with instruments meant for infants twice his size. What followed was a 72-hour vigil where Dr. Çağlar personally monitored every breath, discovering a previously undetected vascular ring compressing the airway. The surgical team he assembled corrected it successfully.

Maya, 11, arrived from a refugee camp with untreated congenital hip dysplasia and spoke no Turkish. Dr. Çağlar learned basic phrases in her language, used drawings to explain the complex surgery, and coordinated with social services for her post-op care. Her first pain-free walk happened in the hospital garden, holding Dr. Çağlar's hand.

As parents of 7-year-old Kemal with severe autism, hospital visits were traumatic until Dr. Çağlar transformed an examination room into a sensory-friendly space with adjustable lighting and quiet instruments. He diagnosed a silent kidney reflux through ultrasound techniques performed while Kemal watched his favorite cartoon. The treatment prevented permanent damage we never knew was occurring.