Hereditary hyperferritinemia cataract syndrome: Case report


Guzelkucuk Z., ÇAKMAKLI H. F. , Onen M., Pietrangelo A., Yarali N.

Gazi Medical Journal, vol.31, no.3, pp.445-446, 2020 (Peer-Reviewed Journal) identifier

  • Publication Type: Article / Article
  • Volume: 31 Issue: 3
  • Publication Date: 2020
  • Doi Number: 10.12996/gmj.2020.108
  • Journal Name: Gazi Medical Journal
  • Journal Indexes: Emerging Sources Citation Index, Scopus, Academic Search Premier
  • Page Numbers: pp.445-446
  • Keywords: cataract, Hyperferritinemia, L-ferritin

Abstract

© 2020 by Gazi University Medical Faculty-Available on-line at web site.Hereditary Hyperferritinemia-Cataract Syndrome (HHCS) is a rare disease characterized by cataract and hyperferritinemia. Herein, we present a pediatric patient diagnosed with HHCS.