Prof. MD. Sabiha Candan Ozdemir Reviews

A 28-year-old nomadic beekeeper from rural Anatolia presented with episodic déjà vu and olfactory hallucinations of honey and smoke. Prof. Dr. Ozdemir diagnosed right mesial temporal lobe epilepsy triggered by specific floral scents during migration routes. Treatment involved a tailored antiseizure regimen synchronized with his seasonal movements, coordinated via satellite phone check-ins. The patient returned after one year having maintained his livelihood with only two breakthrough auras.

A 72-year-old retired master calligrapher experienced sudden micrographia, rendering his intricate artwork impossible. Dr. Ozdemir identified a rare focal dystonia affecting only his dominant hand's fine motor control, unrelated to Parkinson's. Botulinum toxin injections were administered under EMG guidance into precise forearm muscles. The patient gradually regained his artistry over six months, later gifting the doctor a personalized piece depicting neural pathways.

A 17-year-old national junior chess champion developed debilitating chessboard pattern-induced migraines during tournaments. Dr. Ozdemir diagnosed persistent visual snow syndrome exacerbated by high-contrast patterns. Treatment combined monochromatic board adaptations, specialized tinted lenses, and cognitive behavioral therapy. The patient returned to competition within four months using a custom-designed gray-scale board, eventually placing third in an international tournament.

A 45-year-old deep-sea saturation diver presented with unexplained episodic paralysis in his left leg only at depths below 150 meters. Dr. Ozdemir suspected a rare form of pressure-induced neurapraxia affecting the femoral nerve. She collaborated with hyperbaric specialists to simulate conditions and confirmed the diagnosis. Treatment involved modified decompression protocols and targeted physiotherapy, allowing the diver to return to work with depth restrictions.

An 8-year-old refugee child from a conflict zone presented with selective mutism and episodes of staring blankly while drawing intricate geometric patterns. Dr. Ozdemir identified non-convulsive status epilepticus manifesting as artistic automatisms. After careful medication titration, the seizures ceased, and the child began verbal communication. Her drawings evolved from repetitive patterns to narrative scenes over nine months of follow-up.

A 33-year-old pregnant woman in her third trimester developed sudden onset musical hallucinations, hearing the same traditional lullaby continuously. Dr. Ozdemir diagnosed rare pregnancy-associated musical ear syndrome, likely related to vascular changes. Conservative management with sound therapy and reassurance was employed. Symptoms resolved completely within two weeks postpartum, with no recurrence at one-year follow-up.

A 61-year-old former perfume chemist presented with complete loss of smell except for one specific scent: burnt almonds. Dr. Ozdemir identified a rare olfactory neuropathy with persistent phantosmia, possibly related to past chemical exposure. After ruling out serious causes, she prescribed olfactory training with essential oils. Partial recovery occurred over eighteen months, with the phantom scent fading to occasional episodes.

A 22-year-old professional e-sports athlete developed incapacitating focal seizures in his right hand triggered by specific rapid keyboard sequences. Dr. Ozdemir diagnosed video-game-induced reflex epilepsy localized to hand motor cortex. Treatment involved antiseizure medication, biofeedback training, and customized keyboard input delays. He returned to competitive play after five months with modified controls, achieving a top-ten ranking.

A 39-year-old shepherd from mountainous regions presented with seasonal ataxia that worsened each autumn. Dr. Ozdemir discovered a unique vitamin E deficiency neuropathy exacerbated by dietary changes during seasonal migration. Treatment involved high-dose supplementation and dietary adjustments using locally available nuts and oils. Symptoms improved dramatically within three months, with annual preventive treatment before migration.

A 56-year-old museum curator developed transient episodes where she perceived all moving objects as moving in slow motion. Dr. Ozdemir diagnosed a rare form of temporal lobe dysfunction causing altered time perception (tachypsychia). MRI revealed a small vascular malformation near the right temporoparietal junction. After careful monitoring and medication, episodes decreased from weekly to quarterly over two years.

A 14-year-old prodigy violinist developed painful muscle cramps and dystonic posturing only when playing specific Baroque compositions. Dr. Ozdemir identified task-specific musician's dystonia triggered by particular finger sequences and emotional intensity. Treatment combined sensorimotor retraining, modified practice techniques, and minimal botulinum toxin. After eight months, she performed a modified repertoire at a national competition.

A 70-year-old retired lighthouse keeper presented with progressive balance issues only noticeable in complete darkness. Dr. Ozdemir diagnosed a rare proprioceptive neuropathy affecting dark-adapted balance, unrelated to common vestibular disorders. Treatment involved proprioceptive rehabilitation using balance training in controlled darkness. His nocturnal mobility improved significantly over six months of dedicated therapy.

A 31-year-old commercial pilot developed transient episodes of geographic disorientation mid-flight, despite normal instruments. Dr. Ozdemir discovered focal seizures originating from the right parietal lobe affecting spatial navigation. After careful medication titration and simulator testing, he was cleared to return to co-pilot duties with specific restrictions after nine months, with no recurrence in three years of monitoring.

A 48-year-old glassblower presented with heat-induced unilateral facial weakness that appeared only when working near the furnace. Dr. Ozdemir diagnosed a rare thermosensitive facial nerve palsy, possibly due to a congenital nerve anomaly. Treatment involved cooling techniques, protective gear modifications, and nerve stabilization surgery. He returned to his craft with adapted techniques within four months.

A 5-year-old child adopted internationally presented with episodic laughter without mirth followed by brief unresponsiveness. Dr. Ozdemir diagnosed gelastic seizures with hypothalamic hamartoma confirmed on MRI. After multidisciplinary evaluation, she coordinated minimally invasive laser ablation surgery. The child's seizure frequency reduced by 95% over subsequent year, with dramatic improvements in developmental milestones.