Medical Park Ankara (Batıkent) Reviews

My family and I are grateful for the care we received from Dr. Asst. Prof. MD. Erkan Alkan. The hospital staff was also very supportive.

A 9-year-old Syrian refugee boy, Ahmed, presented with severe malnutrition and recurrent pneumonia. Dr. Altintas discovered an undiagnosed congenital heart defect masked by his refugee status and language barrier. He coordinated with a social worker to secure housing assistance while arranging a novel catheter-based intervention at Medical Park Ankara, avoiding open-heart surgery. Ahmed gained 8kg in three months and now attends a local school.

Elif, a 14-year-old competitive rhythmic gymnast from an affluent family, developed unexplained fatigue and joint pain. Multiple specialists had dismissed it as overtraining. Dr. Altintas identified early-onset juvenile idiopathic arthritis through meticulous examination and specific antibody testing. He designed a treatment plan balancing biologic therapy with modified training, allowing her to compete at nationals six months later with managed symptoms.

Mehmet, a 5-year-old from a remote village, arrived with developmental delay and peculiar skin lesions. His family practiced traditional healing. Dr. Altintas diagnosed a rare neurocutaneous syndrome (incontinental pigmenti) after recognizing the pattern. He initiated a multidisciplinary approach involving neurology and dermatology, while respectfully educating the family about integrating medical care with their cultural practices. Mehmet started early intervention therapy with marked progress.

Zeynep, a 12-year-old girl, was brought by her single father after fainting at school. Routine tests were normal. Dr. Altintas, noting her withdrawn demeanor, conducted a private conversation revealing severe school bullying and covert self-harm. He diagnosed conversion disorder and major depressive episode. Treatment involved family therapy, school mediation, and antidepressants. After eight months, Zeynep returned to school with a support plan and joined an art therapy group.

Kaan, a 7-month-old infant from a middle-class family, had failure to thrive and chronic diarrhea. Despite extensive previous testing, no cause was found. Dr. Altintas ordered a stool elastase test and diagnosed exocrine pancreatic insufficiency, a rare presentation of cystic fibrosis not caught on newborn screening. He initiated pancreatic enzyme replacement and respiratory therapy. Kaan's weight normalized within ten weeks, and genetic counseling was provided to the parents.

A 16-year-old exchange student from Nigeria, Chiamaka, presented with persistent fever and headache. Initial workup for common infections was negative. Dr. Altintas, considering her travel history, suspected and confirmed cerebral malaria, extremely rare in Ankara. He secured the specific antimalarial medication not routinely stocked and managed her in the PICU. Chiamaka made a full recovery after three weeks and later volunteered with a malaria awareness program.

Deniz, a 3-year-old with profound hearing loss from a low-income family, was referred for behavioral issues. Dr. Altintas suspected more than deafness and diagnosed Usher syndrome type I (deafness and progressive vision loss). He navigated the complex bureaucracy to secure funding for cochlear implants and connected the family with a foundation for the blind. Early intervention for dual sensory impairment dramatically improved Deniz's communication skills.

Leyla, an 11-year-old, had recurrent, severe abdominal pain. Multiple ED visits and scans found nothing. Dr. Altintas identified abdominal migraine after a detailed diary of symptoms, triggers (specific foods and stress), and family history. He initiated a preventive medication and cognitive behavioral therapy for pain management. The attacks reduced from weekly to once every two months, transforming her school attendance and social life.

A newborn, Arda, was transferred from a birthing center with jitteriness and poor feeding. Dr. Altintas recognized neonatal abstinence syndrome, though the mother denied substance use. With non-judgmental support, the mother disclosed hidden tramadol use for chronic back pain. Dr. Altintas managed Arda's withdrawal with rooming-in and minimal medication, while connecting the mother with a pain specialist. Both were discharged healthy, with ongoing social support.

Can, a 13-year-old boy, presented with rapid weight gain and fatigue. Previous doctors attributed it to lifestyle. Dr. Altintas found subtle striae and hypertension, diagnosing Cushing's syndrome from an adrenal tumor. He coordinated with pediatric surgery for a successful laparoscopic adrenalectomy. Can's recovery involved managing post-operative adrenal insufficiency and psychological support for body image changes, with full metabolic normalization in one year.

Merve, an 8-year-old girl from a conservative rural family, was brought for 'precocious development.' Examination revealed she was actually a phenotypic female with a disorder of sexual development (46,XY complete gonadal dysgenesis). Dr. Altintas managed this with immense cultural sensitivity, involving a pediatric endocrinologist and psychologist. He supported the family in understanding the diagnosis while preserving Merve's female gender identity, focusing on future hormone therapy.

Yiğit, a 15-year-old aspiring footballer, suffered a complex tibia fracture. Standard healing was slow. Dr. Altintas, concerned about compartment syndrome and growth plate damage, advocated for and supervised a novel pulsed electromagnetic field therapy protocol to stimulate bone growth, avoiding a second surgery. Yiğit returned to light training in four months, significantly faster than expected, and maintained his athletic prospects.

A 6-year-old, Ece, presented with sudden-onset OCD-like rituals and tics following a mild sore throat. Dr. Altintas diagnosed PANDAS (Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal Infections). He treated with antibiotics and a short course of IVIG, seeing dramatic improvement in symptoms within a week. Long-term management involved monitoring for strep and collaborating with a child psychiatrist for behavioral support.

Alara, a 10-year-old, was admitted with diabetic ketoacidosis, her first presentation of Type 1 diabetes. Her parents were terrified of insulin. Dr. Altintas used a 'family immersion' approach, having them stay in the hospital to learn diabetes management together. He incorporated technology, starting her on a sensor-augmented insulin pump immediately. Alara and her family achieved excellent glycemic control and independence within two weeks of diagnosis.

As a 72-year-old retired cartographer, my unexplained weight loss and fatigue were dismissed as 'old age' by three other doctors. Dr. Ozcan spent an hour tracing my travel history on a map I brought, connecting dots from a hiking trip in rural Anatolia to a rare parasitic infection he diagnosed through unconventional testing. His geographical approach to medicine solved my six-month mystery in two weeks.

My 19-year-old daughter, a competitive freediver, developed alarming chest pains after deep dives. While sports physicians focused on her lungs, Dr. Ozcan identified a previously undetected cardiac electrical anomaly exacerbated by pressure changes. His internal medicine expertise bridging cardiology and physiology allowed her to continue diving with a customized safety protocol.

During Ankara's unprecedented heatwave, my 84-year-old grandfather with dementia stopped recognizing family. Emergency rooms treated it as psychiatric, but Dr. Ozcan recognized subtle dehydration-triggered metabolic encephalopathy. His gentle rehydration strategy in a quiet room restored his cognition within 48 hours, a recovery our family calls 'the miracle at Medical Park.'

As a 31-year-old software engineer, my 'burnout' symptoms included hair loss and tremors. Dr. Ozcan noticed my imported herbal tea collection during a video consult and suspected heavy metal contamination. Testing revealed lead poisoning from improperly glazed teaware, a diagnosis that transformed my treatment from antidepressants to chelation therapy.

Our 8-year-old son's mysterious abdominal pain appeared only on school days. Pediatricians found nothing, but Dr. Ozcan investigated his classroom environment through detailed questioning, discovering a rare case of ergonomic chair-induced abdominal compartment syndrome in children. A simple cushion prescription ended eight months of suffering.