A case of 14q terminal deletion syndrome and hemifacial microsomia with review of terminal 14q deletion cases

aDepartment of Pediatric Genetics, Necmettin Erbakan University, Faculty of Medicine bDepartment of Medical Genetics, Konya City Hospital, Medical Genetics, Konya, Turkey Received 26 November 2023 Accepted 12 January 2024. Correspondence to Hayriye Nermin Kececi, MD, Departments of Pediatric Genetics, Necmettin Erbakan University, Faculty of Medicine, 42080 Meram, Konya, Turkey Tel: +90 332 223 78 39; fax: +90 332 223 61 81 and +90 332 223 61 82; e-mail: [email protected]