MediFind found 7 doctor with experience in Potter Syndrome near Ankara, TR. Of these, 5 are Experienced and 2 are Advanced.
Ugur Dilmen practices in Tahir, Turkey. Dilmen is rated as an Advanced expert by MediFind in the treatment of Potter Syndrome. Their top areas of expertise are Premature Infant, Patent Ductus Arteriosus, Neonatal Sepsis, and Necrotizing Enterocolitis.
Erdem Fadiloglu practices in Ankara, Turkey. Mr. Fadiloglu is rated as an Advanced expert by MediFind in the treatment of Potter Syndrome. His top areas of expertise are Congenital Muscular Dystrophy Type 1A, Bilateral Renal Agenesis Dominant Type, Potter Syndrome, Lymphadenectomy, and Intrauterine Device Insertion.
Omer Erdeve practices in Mamak, Turkey. Mr. Erdeve is rated as an Experienced expert by MediFind in the treatment of Potter Syndrome. His top areas of expertise are Patent Ductus Arteriosus, Premature Infant, Newborn Transient Tachypnea, and Infant Respiratory Distress Syndrome.
Canan Unal practices in Ankara, Turkey. Mr. Unal is rated as an Experienced expert by MediFind in the treatment of Potter Syndrome. His top areas of expertise are Congenital Muscular Dystrophy Type 1A, Glycogen Storage Disease Type 6, Potter Syndrome, Hysterectomy, and Splenectomy.
S Oguz practices in Ankara, Turkey. Oguz is rated as an Experienced expert by MediFind in the treatment of Potter Syndrome. Their top areas of expertise are Premature Infant, Infant Respiratory Distress Syndrome, Intraventricular Hemorrhage of the Newborn, and Necrotizing Enterocolitis.
Meral Beksac practices in Ankara, Turkey. Ms. Beksac is rated as an Experienced expert by MediFind in the treatment of Potter Syndrome. Her top areas of expertise are Multiple Myeloma, Plasmacytoma, Chronic Graft Versus Host Disease (cGvHD), Bone Marrow Aspiration, and Bone Marrow Transplant.
Murat Cagan practices in Ankara, Turkey. Mr. Cagan is rated as an Experienced expert by MediFind in the treatment of Potter Syndrome. His top areas of expertise are Potter Syndrome, Bilateral Renal Agenesis Dominant Type, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, and Diastasis Recti.
Last Updated: 01/09/2026