Hereditary Hyperferritinemia Cataract Syndrome: Case Report

Kalıtsal Hiperferritinemi Katarakt Sendromu

Authors

  • Zeliha Guzelkucuk Kırşehir Ahi Evran University Training and Research Hospital
  • Hasan Fatih Çakmaklı
  • Mehmet Onen Numune Training and Research Hospital, Department of Ophthalmology, Ankara, Turkey
  • Antonello Pietrangelo 4University Hospital of Modena, Unit of Internal Medicine and Metabolic Diseases Center for Hemochromatosis, Modena, İtalya
  • Nese Yaralı University of Health Sciences, Ankara City Hospital, Department of Pediatric Hematology and Oncology

Abstract

Hereditary Hyperferritinemia-Cataract Syndrome (HHCS) is a rare disease characterized by cataract and hyperferritinemia. Herein, we present a pediatric patient diagnosed with HHCS.

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Published

11.06.2020

Issue

Vol. 31 No. 3 (2020): Gazi Medical Journal

Section

Case Report