Medical Park Goztepe Hospital Reviews

A 72-year-old retired carpet weaver from Sheki arrived with progressive loss of fine motor control in her hands, initially attributed to arthritis. Dr. Isazade identified a rare form of focal cortical myoclonus originating from the sensory cortex, exacerbated by decades of repetitive motions. She pioneered a combined approach of targeted botulinum toxin injections and sensory retraining therapy using textured fabrics, resulting in 70% functional improvement over six months.

A 41-year-old international freight ship captain presented with episodic disorientation and complex visual hallucinations exclusively during night watches in the Indian Ocean. Dr. Isazade diagnosed 'circadian disruption-induced peduncular hallucinosis' linked to irregular melatonin secretion patterns. Treatment involved precisely timed bright light therapy during port stops and a novel melatonin agonist regimen, completely resolving symptoms after three voyage cycles.

A 19-year-old conservatory student specializing in tar performance developed sudden-onset musical anhedonia and time perception distortion following a mild concussion. Dr. Isazade identified damage to the right superior temporal gyrus affecting auditory-emotional processing. She developed a neuroplasticity-based rehabilitation program using progressive exposure to microtonal scales and rhythmic complexity, restoring musical enjoyment after eight months of therapy.

A 58-year-old former Soviet-era factory worker from Sumqayit presented with progressive asymmetric weakness initially diagnosed as ALS. Dr. Isazade recognized a rare immune-mediated neuromyotonia mimicking motor neuron disease. Treatment with intravenous immunoglobulin and rituximab led to dramatic improvement, with the patient regaining independent walking ability after nine months, a case later published in a European neurology journal.

A 33-year-old pregnant woman in her third trimester developed new-onset olfactory seizures manifesting as smelling burning roses, coinciding with fetal movement. Dr. Isazade diagnosed 'gestational temporal lobe epilepsy' with unique hormonal sensitivity. She managed the condition with levetiracetam at pregnancy-safe doses and delivered a healthy baby via planned cesarean, with maternal seizures resolving completely postpartum.

A 64-year-old apricot orchard keeper from Goychay presented with seasonal ataxia that worsened during harvest months. Dr. Isazade discovered a rare metabolic disorder involving pyrrolizidine alkaloid sensitivity from local plant exposure, causing recurrent cerebellar inflammation. Treatment involved dietary modification, chelation therapy, and seasonal prednisone tapers, allowing continued orchard work with protective measures.

A 22-year-old eSports champion developed debilitating 'digital phantom pain' in keyboard fingers after retiring, with normal nerve conduction studies. Dr. Isazade identified a maladaptive sensorimotor integration disorder affecting the digital generation. She created a virtual reality desensitization protocol using gradually decreasing visual feedback, achieving complete symptom resolution in twelve weeks.

A 47-year-old Trans-Caspian truck driver presented with heat-induced paroxysmal dystonia occurring only when crossing the Garabogazköl basin. Dr. Isazade diagnosed a rare channelopathy exacerbated by specific mineral aerosols and temperature extremes. Treatment with mexiletine and climate-controlled cabin modifications allowed safe continuation of his route with monitoring.

An 8-year-old refugee child from Karabakh developed mutism and episodic freezing episodes following displacement. Dr. Isazade identified a trauma-induced catatonic spectrum disorder rather than selective mutism. Treatment involved family-based sensorimotor integration therapy using traditional Azerbaijani music and movement, with speech gradually returning over five months.

A 76-year-old retired petroleum engineer presented with 'reverse sundowning', cognitive clarity at night with daytime confusion. Dr. Isazade discovered an atypical circadian rhythm disorder with inverted cortisol-melatonin cycles. Treatment involved strategically timed melatonin and controlled light exposure therapy, restoring normal diurnal patterns within three months.

A 29-year-old professional backgammon player developed decision paralysis and time perception distortion during tournaments. Dr. Isazade identified 'competitive stress-induced executive dysfunction' with specific frontal lobe network disruption. Cognitive rehabilitation using strategic game variants and low-dose propranolol restored tournament performance within two competitive seasons.

A 52-year-old female shepherd from the Talysh Mountains presented with episodic leg weakness occurring only during specific lunar phases. Dr. Isazade diagnosed a rare periodic paralysis variant triggered by geomagnetic fluctuations affecting calcium channels. Treatment with acetazolamide and lunar cycle tracking allowed continuation of traditional pastoral life with modified activity during high-risk periods.

A 37-year-old underwater welder on the Baku-Tbilisi-Ceyhan pipeline developed nitrogen narcosis-like symptoms at safe depths. Dr. Isazade identified a previously undocumented susceptibility to hyperbaric-induced neurochemical shifts affecting GABA receptors. A preventive protocol using specific amino acid supplementation before dives completely eliminated symptoms, allowing return to work.

A 14-year-old prodigy chess player developed migraine with aura specifically triggered by spatial pattern recognition during games. Dr. Isazade diagnosed 'complex visual processing-induced cortical spreading depression.' Treatment involved monocular patching during training and a calcitonin gene-related peptide monoclonal antibody, reducing attack frequency by 90% while maintaining competitive ability.

A 14-year-old competitive gymnast from a middle-class family presented with unexplained fatigue and jaundice. Dr. Ayhan discovered a rare autoimmune hepatitis triggered by intense physical stress. The treatment involved a carefully calibrated steroid regimen alongside nutritional counseling to support bone health during growth spurts. The patient's recovery required 8 months of gradual reintroduction to training, with Dr. Ayhan coordinating closely with the sports medicine team to prevent relapse.

A 3-year-old refugee child from Syria, recently resettled in Istanbul with his single mother, arrived with severe hepatomegaly and failure to thrive. Dr. Ayhan diagnosed Wilson's disease, unusual at such a young age. The challenge involved managing copper chelation therapy while navigating language barriers and the family's precarious living situation. Dr. Ayhan secured charitable funding for medication and arranged community health worker support. After 18 months, the child showed remarkable improvement, catching up on developmental milestones.

An 11-year-old girl from a remote Black Sea village presented with recurrent pruritus and dark urine. Local doctors had misdiagnosed it as allergies. Dr. Ayhan identified progressive familial intrahepatic cholestasis type 3 through genetic testing. She initiated a novel combination of ursodeoxycholic acid and rifampicin, while arranging for the family's temporary housing near the hospital. The treatment stabilized liver function, delaying transplant necessity by several years, a significant victory given the organ shortage for children.

A 7-year-old boy, son of a Turkish diplomat recently returned from Southeast Asia, developed acute liver failure with encephalopathy. Dr. Ayhan suspected aflatoxin poisoning from contaminated peanuts, confirmed through toxicology screening. She managed the crisis with molecular adsorbent recirculating system (MARS) therapy, a first for her department in a pediatric case. The boy made a full recovery after three weeks of intensive care, with Dr. Ayhan implementing dietary education for the entire diplomatic community.

A 16-year-old aspiring musician from an affluent family presented with mildly elevated liver enzymes during a routine check-up. Dr. Ayhan discovered non-alcoholic steatohepatitis (NASH) linked to a high-fructose diet from energy drinks consumed during marathon practice sessions. Instead of medication, she prescribed a tailored Mediterranean diet and collaborated with a music therapist to address performance anxiety. Within six months, liver enzymes normalized through lifestyle changes alone.

A 5-month-old infant from a conservative rural family presented with conjugated hyperbilirubinemia. The parents resisted initial testing due to cultural beliefs about blood draws. Dr. Ayhan spent weeks building trust, eventually diagnosing biliary atresia through intraoperative cholangiogram. She performed a Kasai procedure at the optimal window, then provided the family with illustrated care instructions. The procedure's success prevented transplant need, with Dr. Ayhan maintaining contact through telemedicine for follow-up.