ABSTRACT
Hereditary Hyperferritinemia-Cataract Syndrome (HHCS) is a rare disease characterized by cataract and hyperferritinemia. Herein, we present a pediatric patient diagnosed with HHCS.
Hereditary Hyperferritinemia Cataract Syndrome: Case Report
GMJ 2020;31(3):445-446
1. University of Health Sciences, Ankara City Hospital, Department of Pediatric Hematology and Oncology, Ankara, Turkey
2. Ankara University, Faculty of Medicine, Department of Pediatric Hematology and Oncology, Ankara, Turkey
3. Numune Training and Research Hospital, Department of Ophthalmology, Ankara, Turkey
4. University Hospital of Modena, Unit of Internal Medicine and Metabolic Diseases Center for Hemochromatosis, Modena, İtalya
5. Yıldırım Beyazıt University, Ankara City Hospital, Department of Pediatric Hematology and Oncology, Ankara, Turkey
No information available.
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Received Date: 06.02.2020
Accepted Date: 11.05.2020
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