Memorial Göztepe Hospital
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Professor Zafer Gülbaş — hematologist-oncologist, founder and director of the Bone Marrow Transplant Center at Anadolu Medical Center, which is among the largest in Europe.
Why patients choose and trust Dr. Gülbaş:
Dr. Haluk Cokugras is a pediatric specialist at Memorial Göztepe Hospital (2025–present). He previously served in the Department of Pediatrics at Istanbul University, Cerrahpaşa Faculty of Medicine (1983–2024).
He earned his MD from Istanbul University, Cerrahpaşa Faculty of Medicine (1975–1981). He later completed specialization in pediatrics (1988), pediatric allergy (1998–2001), and pediatric infectious diseases (2004).
Professional memberships: Turkish Pediatric Association; Pediatric Allergy, Immunology and Asthma Association; Pediatric Infectious Diseases Association; Balkan Pediatric Society; European Academy of Allergy and Clinical Immunology. He has attended Turkish Pediatrics, Pediatric Allergy, Pediatric Infectious Diseases, and Pediatric Pulmonology congresses.
Specialized Turkish hospitals like Anadolu Medical Center and Acibadem Altunizade offer advanced Fanconi Anemia care. These centers feature dedicated hematology-oncology departments and bone marrow transplant units. Many maintain Joint Commission International accreditation and specific European Blood and Marrow Transplantation certifications for complex marrow failure syndromes.
Bookimed Expert Insight: Success in Fanconi Anemia depends on experience with allogeneic transplants for inherited syndromes. Anadolu Medical Center reports an 81% success rate for autologous transplants specifically. This high volume often leads to better management of the unique conditioning regimens required. Dr. Zafer Gulbas leads these efforts, bringing expertise from top global institutions like M.D. Anderson.
Patient Consensus: Patients emphasize finding teams experienced in inherited marrow failure rather than general oncology. They note that coordinating with genetics and fertility counseling is vital for long-term care.
Turkish centers treat Fanconi Anemia through curative hematopoietic stem cell transplantation. Specialized units at Anadolu Medical Center utilize protocols from Johns Hopkins Medicine. Options include matched sibling and unrelated donor transplants. Centers provide androgen therapy and leukodepleted transfusions to manage bone marrow failure before surgery.
Bookimed Expert Insight: Anadolu Medical Center stands out because Dr. Zafer Gulbas has performed over 3,300 procedures. This high volume is critical for Fanconi Anemia cases. Such rare conditions require surgeons who manage thousands of transplants to ensure safety. The center's partnership with Johns Hopkins provides access to specialized reduced-intensity conditioning protocols.
Patient Consensus: Families emphasize finding centers with dedicated pediatric hematology programs for long-term monitoring. Patients note that starting leukodepleted transfusions early helps avoid complications during the eventual transplant process.
Turkish referral centers report overall survival rates for Fanconi anemia patients exceeding 70% to 80% following bone marrow transplantation. Success hinges on specialized reduced-intensity conditioning regimens. Leading facilities like ACIBADEM report survival rates near 85% by using advanced haploidentical and unrelated donor transplant techniques.
Bookimed Expert Insight: Success often depends on cumulative institutional experience rather than just technology. For example, Dr. Zafer Gulbas at Anadolu Medical Center has overseen 3,000+ transplants since 2010. This high volume allows centers to refine the delicate conditioning balance required for Fanconi anemia patients.
Turkish physicians are highly proficient in treating Fanconi Anemia through specialized hematology and bone marrow transplant centers. Experts like Dr. Zafer Gulbas have performed over 3,000 transplants since 2010. Turkish facilities often use Johns Hopkins Medicine International protocols for managing complex genetic blood disorders.
Bookimed Expert Insight: Turkish hematology centers see higher volumes of Fanconi Anemia than many European facilities. This stems from local genetic prevalence reaching 78% in certain patient groups. Dr. Zafer Gulbas alone has over 260 publications and 5,000 citations on blood disorders. This volume creates a concentrated expertise in managing the unique toxicity risks of Fanconi Anemia.
Patient Consensus: Patients emphasize finding a center that coordinates with medical genetics for family screening. They note that successful treatment requires a team familiar with specific Fanconi Anemia transplant preparation protocols.
Post-transplant follow-up for international Fanconi Anemia patients in Turkey requires intensive monitoring of donor engraftment and graft-versus-host disease (GVHD). Care lasts for several years and involves frequent bloodwork and immunosuppression management. Turkey's leading hematology centers maintain long-term coordination with home-country doctors to ensure patient safety.
Bookimed Expert Insight: Turkish hematology centers often require international patients to stay nearby for 3–4 months post-discharge. Dr. Zafer Gulbas at Anadolu Medical Center has performed over 3,300 procedures, emphasizing why experienced teams prioritize this period. This extended stay allows for rapid adjustments that standard local clinics might miss.
Patient Consensus: Patients note that recovery is a slow rebuild rather than a quick return to normal life. Coordination between the Turkish center and local doctors is the most critical factor for long-term health.