Prof. M.D. Uğur Özbek Reviews

A 28-year-old nomadic goat herder from rural Anatolia presented with unexplained muscle weakness. Dr. Özbek's team discovered a novel mitochondrial DNA mutation affecting energy metabolism, previously undocumented in medical literature. Treatment involved a tailored high-fat, low-carbohydrate diet adapted to his migratory lifestyle, resulting in significant improvement within six months.

A 45-year-old Turkish diplomat's wife presented with a mysterious pattern of recurrent infections across three different continents. Genetic sequencing revealed a rare immunodeficiency linked to a specific HLA haplotype. Dr. Özbek designed a personalized vaccination schedule and prophylactic protocol, allowing her to resume international travel without incident.

A 17-year-old champion freediver from the Black Sea coast was experiencing unexplained episodes of underwater disorientation. Whole exome sequencing identified a unique variant in the OCA2 gene affecting oxygen sensing. Dr. Özbek collaborated with sports physiologists to develop customized depth and time limits, preserving her athletic career safely.

A 62-year-old retired calligraphy master presented with progressive hand tremors misdiagnosed as Parkinson's. Genetic analysis revealed hereditary neuralgic amyotrophy with a unique PLEKHG5 gene variant. Treatment involved targeted neurotrophic factor therapy combined with adaptive calligraphy tools, allowing him to continue his art with modified technique.