Abstract
Hereditary Hyperferritinemia-Cataract Syndrome (HHCS) is a rare disease characterized by cataract and hyperferritinemia. Herein, we present a pediatric patient diagnosed with HHCS.
Keywords: Hyperferritinemia, cataract, L-Ferritin
Hereditary Hyperferritinemia Cataract Syndrome: Case Report
Case Report
Hereditary Hyperferritinemia Cataract Syndrome: Case Report
Gazi Med J 2020;31(3):445-446· DOI: 10.12996/gmj.2020.108
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- 1University of Health Sciences, Ankara City Hospital, Department of Pediatric Hematology and Oncology, Ankara, Turkey
- 2Ankara University, Faculty of Medicine, Department of Pediatric Hematology and Oncology, Ankara, Turkey
- 3Numune Training and Research Hospital, Department of Ophthalmology, Ankara, Turkey
- 4University Hospital of Modena, Unit of Internal Medicine and Metabolic Diseases Center for Hemochromatosis, Modena, İtalya
- 5Yıldırım Beyazıt University, Ankara City Hospital, Department of Pediatric Hematology and Oncology, Ankara, Turkey
Corresponding Author: Zeliha Guzelkuçuk — drguzelkucuk@hotmail.com
Received06.02.2020Accepted11.05.2020
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